[ CAS No. 3572-64-3 ] {[proInfo.proName]}

Name: 3572-64-3|2-(3-Oxo-2-pentylcyclopentyl)acetic acid|98%
Brand: Ambeed
SKU: A1493332
Rating: 94 (32 reviews)

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Cat. No.: {[proInfo.prAm]}

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Structure of 3572-64-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 3572-64-3 ]

COA NMR CNMR HPLC LC-MS

Related Doc. of [ 3572-64-3 ]

SDS Specification

Alternatived Products of [ 3572-64-3 ]

Product Details of [ 3572-64-3 ]

CAS No. :	3572-64-3	MDL No. :	MFCD18781916
Formula :	C₁₂H₂₀O₃	Boiling Point :	-
Linear Structure Formula :	-	InChI Key :	PQEYTAGBXNEUQL-UHFFFAOYSA-N
M.W :	212.29	Pubchem ID :	107126
Synonyms :	(±)-9,10-Dihydrojasmonic Acid	Chemical Name :	2-(3-Oxo-2-pentylcyclopentyl)acetic acid

Calculated chemistry of [ 3572-64-3 ]

Physicochemical Properties

Num. heavy atoms :	14
Num. arom. heavy atoms :	0
Fraction Csp3 :	0.82
Num. rotatable bonds :	5
Num. H-bond acceptors :	3.0
Num. H-bond donors :	1.0
Molar Refractivity :	54.85
TPSA :	54.37 Å²

Pharmacokinetics

GI absorption :	High
BBB permeant :	Yes
P-gp substrate :	No
CYP1A2 inhibitor :	No
CYP2C19 inhibitor :	No
CYP2C9 inhibitor :	No
CYP2D6 inhibitor :	No
CYP3A4 inhibitor :	No
Log Kp (skin permeation) :	-6.2 cm/s

Lipophilicity

Log Po/w (iLOGP) :	1.64
Log Po/w (XLOGP3) :	1.85
Log Po/w (WLOGP) :	2.25
Log Po/w (MLOGP) :	1.49
Log Po/w (SILICOS-IT) :	2.21
Consensus Log Po/w :	1.89

Druglikeness

Lipinski :	0.0
Ghose :	None
Veber :	0.0
Egan :	0.0
Muegge :	1.0
Bioavailability Score :	0.56

Water Solubility

Log S (ESOL) :	-1.9
Solubility :	2.47 mg/ml ; 0.0125 mol/l
Class :	Very soluble
Log S (Ali) :	-2.61
Solubility :	0.484 mg/ml ; 0.00244 mol/l
Class :	Soluble
Log S (SILICOS-IT) :	-2.08
Solubility :	1.65 mg/ml ; 0.0083 mol/l
Class :	Soluble

Medicinal Chemistry

PAINS :	0.0 alert
Brenk :	0.0 alert
Leadlikeness :	1.0
Synthetic accessibility :	2.66

Safety of [ 3572-64-3 ]

Signal Word:	Danger	Class:	8
Precautionary Statements:	P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313	UN#:	3265
Hazard Statements:	H315-H318	Packing Group:	Ⅲ
GHS Pictogram:

Application In Synthesis of [ 3572-64-3 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

Upstream synthesis route of [ 3572-64-3 ]
Downstream synthetic route of [ 3572-64-3 ]

[ 3572-64-3 ] Synthesis Path-Upstream 1~2

1
[ 51806-23-6 ]
[ 24851-98-7 ]
[ 3572-64-3 ]

Yield	Reaction Conditions	Operation in experiment
90.7%	at 180 - 215℃; for 4 - 16 h;	A 1 L four-neck flask equipped with a stirrer, a supply unit, a thermometer and a rectifier was charged with 600 g of raw material containing 545 g (1.92 mol) of dimethyl 2-pentyl-3-oxo-cyclopentylmalonate produced in the same manner as in Production Example 1 and the raw material was heated to 180°C with stirring under normal pressure. Then, the supply of water to the bottom of the reactor was started. During the supply of water, the supply rate of water was adjusted to 6 g/h from the start of the supply to the 2nd hour, to 3 g/h from the 2nd hour to the 8th hour and to 1.2 g/h after the 8th hour with measuring the content of water in the reaction solution by a Karl Fischer's coulometric titration (instrument: Trace-water measuring device AQ-7, manufactured by HIRANUMA SANGYO Co. , Ltd.) such that the content of water was limited to 0.4percent by weight or less. Then, the reaction was completed for 16 hours from the start of the supply of water. The maximum water concentration in the reaction solution was 0.21percent by weight. During the reaction, the difference (X-Y) between the integrating molar number X (excluding distilled water content) of the water to be supplied and the molar number Y of the water reacted with dimethyl 2-pentyl-3-oxo-cyclopentylmalonate was 14.8percent at a maximum based on the molar number of the charged dimethyl 2-pentyl-3-oxo-cyclopentylmalonate. It was found that the reaction product contained 423 g (1.87 mol, yield: 97.3percent) of methyl 2-pentyl-3-oxo-cyclopentylacetate and 10.8 g (0.051 mol) of 2-pentyl-3-oxo-cyclopentylacetic acid.; Comparative Example 1 The same 1 L four-neck flask that was used in Example 1 was charged with 600 g of raw material containing 557 g (1.96 mol) of dimethyl 2-pentyl-3-oxo-cyclopentylmalonate produced in the same manner as in Production Example 1 and the raw material was heated to 180°C with stirring under normal pressure. Then, the supply of water to the bottom of the reactor was started. During the supply of water, the supply rate of water was adjusted to a constant rate (6 g/h) . Then, the reaction was completed for 9 hours from the start of the supply of water. During the supply of water, the content of water in the reaction solution was measured by a Karl Fischer's coulometric titration (instrument: Trace-water measuring device AQ-7, manufactured by HIRANUMA SANGYO Co. , Ltd.) and as a result, the maximum water concentration in the reaction solution was 0.44percent by weight. It was found that the reaction product contained 402 g (1.78 mol, yield: 90.7percent) of methyl 2-pentyl-3-oxo-cyclopentylacetate and 33.5 g (0.158 mol) of 2-pentyl-3-oxo-cyclopentylacetic acid.; Example 2 The same 1 L four-neck flask that was used in Example 1 was charged with 600 g of raw material containing 550 g (1.94 mol) of dimethyl 2-pentyl-3-oxo-cyclopentylmalonate produced in the same manner as in Production Example 1 and the raw material was heated to 215°C with stirring under normal pressure. Then, the supply of water to the bottom of the reactor was started. During the supply of water, the supply rate of water was adjusted to 18 g/h from the start of the supply to the 1st hour, to 12 g/h from the 1st hour to the 2nd hour, to 6 g/h from the 2nd hour to the 3rd hour and to 3 g/h after the 3rd hour with measuring the content of water in the reaction solution by a Karl Fischer' s coulometric titration (instrument: Trace-water measuring device AQ-7, manufactured by HIRANUMA SANGYO Co. , Ltd.) such that the content of water was limited to 0.4percent by weight or less. Then, the reaction was completed for 4 hours from the start of the supply of water. The maximum water concentration in the reaction solution was 0.14percent by weight. During the reaction, the difference (X-Y) between the integrating molar number X (excluding distilled water content) of the water to be supplied and the molar number Y of the water reacted with dimethyl 2-pentyl-3-oxo-cyclopentylmalonate was 10.3percent at a maximum based on the molar number of the supplied dimethyl 2-pentyl-3-oxo-cyclopentylmalonate. It was found that the reaction product contained 420 g (1.86 mol, yield: 96.0percent) of methyl 2-pentyl-3-oxo-cyclopentylacetate and 5.8 g (0.027 mol) of 2-pentyl-3-oxo-cyclopentylacetic acid.

Reference： [1] Patent: EP1498407, 2005, A1, . Location in patent: Page/Page column 6-7

2
[ 186581-53-3 ]
[ 3572-64-3 ]
[ 24851-98-7 ]

Reference： [1] Tetrahedron Letters, 1980, vol. 21, p. 1475 - 1478

[ 3572-64-3 ] Synthesis Path-Downstream 1~24

1
[ 186581-53-3 ]
[ 3572-64-3 ]
[ 24851-98-7 ]

Reference： [1]Tetrahedron Letters,1980,vol. 21,p. 1475 - 1478

2
3-Hydroxymethyl-2-pentyl-cyclopentanol [ No CAS ]
[ 3572-64-3 ]

Reference： [1]Tetrahedron Letters,1980,vol. 21,p. 1475 - 1478

3
[ 67-56-1 ]
[ 3572-64-3 ]
[ 2570-03-8 ]

Reference： [1]Journal of Organic Chemistry,1974,vol. 39,p. 2637 - 2639

4
[ 51806-23-6 ]
[ 3572-64-3 ]

Reference： [1]Journal of Organic Chemistry,1974,vol. 39,p. 2637 - 2639

6
[ 186581-53-3 ]
[ 3572-64-3 ]
[ 2570-03-8 ]
[ 2570-03-8 ]

Reference： [1]European Journal of Organic Chemistry,2001,p. 3837 - 3841

7
[ 42607-76-1 ]
[ 3572-64-3 ]

Reference： [1]European Journal of Organic Chemistry,2001,p. 3837 - 3841

8
[ 25564-22-1 ]
[ 3572-64-3 ]

Reference： [1]European Journal of Organic Chemistry,2001,p. 3837 - 3841
[2]Journal of Organic Chemistry,1974,vol. 39,p. 2637 - 2639

9
2-pentyl-3-(2-propen-1-yl)cyclopentanone [ No CAS ]
[ 3572-64-3 ]

Reference： [1]European Journal of Organic Chemistry,2001,p. 3837 - 3841

10
[ 110-53-2 ]
[ 3572-64-3 ]

Reference： [1]Tetrahedron Letters,1980,vol. 21,p. 1475 - 1478

11
[ 75351-26-7 ]
[ 3572-64-3 ]

Reference： [1]Tetrahedron Letters,1980,vol. 21,p. 1475 - 1478

12
[ 75351-23-4 ]
[ 3572-64-3 ]

Reference： [1]Tetrahedron Letters,1980,vol. 21,p. 1475 - 1478

13
[ 82259-82-3 ]
[ 3572-64-3 ]

Reference： [1]Tetrahedron Letters,1980,vol. 21,p. 1475 - 1478

14
[ 75983-90-3 ]
[ 3572-64-3 ]

Reference： [1]Tetrahedron Letters,1980,vol. 21,p. 1475 - 1478

15
[ 110-53-2 ]
1.3-dithiolane [ No CAS ]
[ 3572-64-3 ]

Reference： [1]Journal of Organic Chemistry,1974,vol. 39,p. 2637 - 2639

16
[ 24851-93-2 ]
[ 3572-64-3 ]

Reference： [1]Journal of Organic Chemistry,1974,vol. 39,p. 2637 - 2639

17
[ 4819-67-4 ]
[ 3572-64-3 ]

Reference： [1]Journal of Organic Chemistry,1974,vol. 39,p. 2637 - 2639

18
[ 24852-03-7 ]
[ 3572-64-3 ]

Reference： [1]Journal of Organic Chemistry,1974,vol. 39,p. 2637 - 2639

19
[ 611-10-9 ]
[ 3572-64-3 ]

Reference： [1]Journal of Organic Chemistry,1974,vol. 39,p. 2637 - 2639

20
[ 51806-23-6 ]
[ 24851-98-7 ]
[ 3572-64-3 ]

Yield	Reaction Conditions	Operation in experiment
90.7 - 97.3%	With water; at 180 - 215℃; for 4 - 16h;Product distribution / selectivity;	A 1 L four-neck flask equipped with a stirrer, a supply unit, a thermometer and a rectifier was charged with 600 g of raw material containing 545 g (1.92 mol) of dimethyl 2-pentyl-3-oxo-cyclopentylmalonate produced in the same manner as in Production Example 1 and the raw material was heated to 180C with stirring under normal pressure. Then, the supply of water to the bottom of the reactor was started. During the supply of water, the supply rate of water was adjusted to 6 g/h from the start of the supply to the 2nd hour, to 3 g/h from the 2nd hour to the 8th hour and to 1.2 g/h after the 8th hour with measuring the content of water in the reaction solution by a Karl Fischer's coulometric titration (instrument: Trace-water measuring device AQ-7, manufactured by HIRANUMA SANGYO Co. , Ltd.) such that the content of water was limited to 0.4% by weight or less. Then, the reaction was completed for 16 hours from the start of the supply of water. The maximum water concentration in the reaction solution was 0.21% by weight. During the reaction, the difference (X-Y) between the integrating molar number X (excluding distilled water content) of the water to be supplied and the molar number Y of the water reacted with dimethyl 2-pentyl-3-oxo-cyclopentylmalonate was 14.8% at a maximum based on the molar number of the charged dimethyl 2-pentyl-3-oxo-cyclopentylmalonate. It was found that the reaction product contained 423 g (1.87 mol, yield: 97.3%) of methyl 2-pentyl-3-oxo-cyclopentylacetate and 10.8 g (0.051 mol) of 2-pentyl-3-oxo-cyclopentylacetic acid.; Comparative Example 1 The same 1 L four-neck flask that was used in Example 1 was charged with 600 g of raw material containing 557 g (1.96 mol) of dimethyl 2-pentyl-3-oxo-cyclopentylmalonate produced in the same manner as in Production Example 1 and the raw material was heated to 180C with stirring under normal pressure. Then, the supply of water to the bottom of the reactor was started. During the supply of water, the supply rate of water was adjusted to a constant rate (6 g/h) . Then, the reaction was completed for 9 hours from the start of the supply of water. During the supply of water, the content of water in the reaction solution was measured by a Karl Fischer's coulometric titration (instrument: Trace-water measuring device AQ-7, manufactured by HIRANUMA SANGYO Co. , Ltd.) and as a result, the maximum water concentration in the reaction solution was 0.44% by weight. It was found that the reaction product contained 402 g (1.78 mol, yield: 90.7%) of methyl 2-pentyl-3-oxo-cyclopentylacetate and 33.5 g (0.158 mol) of 2-pentyl-3-oxo-cyclopentylacetic acid.; Example 2 The same 1 L four-neck flask that was used in Example 1 was charged with 600 g of raw material containing 550 g (1.94 mol) of dimethyl 2-pentyl-3-oxo-cyclopentylmalonate produced in the same manner as in Production Example 1 and the raw material was heated to 215C with stirring under normal pressure. Then, the supply of water to the bottom of the reactor was started. During the supply of water, the supply rate of water was adjusted to 18 g/h from the start of the supply to the 1st hour, to 12 g/h from the 1st hour to the 2nd hour, to 6 g/h from the 2nd hour to the 3rd hour and to 3 g/h after the 3rd hour with measuring the content of water in the reaction solution by a Karl Fischer' s coulometric titration (instrument: Trace-water measuring device AQ-7, manufactured by HIRANUMA SANGYO Co. , Ltd.) such that the content of water was limited to 0.4% by weight or less. Then, the reaction was completed for 4 hours from the start of the supply of water. The maximum water concentration in the reaction solution was 0.14% by weight. During the reaction, the difference (X-Y) between the integrating molar number X (excluding distilled water content) of the water to be supplied and the molar number Y of the water reacted with dimethyl 2-pentyl-3-oxo-cyclopentylmalonate was 10.3% at a maximum based on the molar number of the supplied dimethyl 2-pentyl-3-oxo-cyclopentylmalonate. It was found that the reaction product contained 420 g (1.86 mol, yield: 96.0%) of methyl 2-pentyl-3-oxo-cyclopentylacetate and 5.8 g (0.027 mol) of 2-pentyl-3-oxo-cyclopentylacetic acid.

Reference： [1]Patent: EP1498407,2005,A1 .Location in patent: Page/Page column 6-7

21
[ 24851-98-7 ]
[ 3572-64-3 ]

Yield	Reaction Conditions	Operation in experiment
> 99%		Sodium hydroxide pellets (82.6g) were dissolved in methanol (425 ml) with stirring. This solution was added to a stirred solution of methyldihydrojasmonate (425g)(obtained from F. D. Copeland) in methanol (425 ml). The reaction mixture was stirred at room temperature for 24 hours. After this time TLC analysis (10:90 ethylacetate EtOAc):Hexane) confirmed that all starting material had been consumed. Aqueous 1M hydrochloric acid solution was added slowly until the pH of the reaction mixture was ~1. The aqueous/methanol solution was extracted with ethyl acetate (4 x 150 ml) and the combined organic extracts were dried (MgS04) and evaporated under vacuum to give the dihydrojasmonic acid as a pale yellow oil (397.0g,>99%). The structure was confirmed using ¹H and ¹3C NMR.

Reference： [1]Patent: WO2005/102047,2005,A1 .Location in patent: Page/Page column 14

22
[ 3572-64-3 ]
dihydrojasmonic acid magnesium salt [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	With magnesium methanolate; In methanol; at 20℃;Heating / reflux;	A two-necked 3L round bottom flask was charged with magnesium turnings and methanol (700 ml) under nitrogen. Two crystals of iodine were added. Once the reaction had initiated stirring was commenced and the reaction mixture brought to reflux. The initially dark brown reaction mixture gradually became paler yellow in colour and a white precipitate began to form. Heating was continued until all the magnesium had reacted. At this point the reaction mixture consisted of a virtually colourless solution containing a white precipitate. The reaction mixture was cooled to room temperature before a solution of <strong>[3572-64-3]dihydrojasmonic acid</strong> (350g) in methanol (700 ml) was added dropwise. The reaction mixture was then brought back to reflux, maintained at this temperature for two hours, and then stirred at room temperature overnight. This gave the reaction mixture as a clear pale yellow solution. The methanol was removed under vacuum to give the product as a pale yellow oil. Propan-2-ol (2 x 250 ml) was added and removed under vacuum to remove any residual water and this afforded the <strong>[3572-64-3]dihydrojasmonic acid</strong> magnesium salt (368g, >99%) as a pale yellow solid. The structure was confirmed using ¹H and ¹3C NMR. The ¹H NMR of the magnesium salt showed that the compound contained water. Karl Fisher analysis confirmed this and showed that the magnesium salt contained 1.8% water and residual propan-2-ol.

Reference： [1]Patent: WO2005/102047,2005,A1 .Location in patent: Page/Page column 17

23
[ 3572-64-3 ]
dihydrojasmonic acid potassium salt [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	With potassium hydroxide; In water;Product distribution / selectivity;	Potassium hydroxide (5.29g) was dissolved in water (225ml) with stirring. This was added to the <strong>[3572-64-3]dihydrojasmonic acid</strong> (20g) prepared as described in step 1 to give a 10% wt aqueous solution of the dihydrojasmonic potassium salt. The structure was confirmed using ¹H and ¹3C NMR.

Reference： [1]Patent: WO2005/102047,2005,A1 .Location in patent: Page/Page column 15

24
[ 3572-64-3 ]
C₁₂H₁₉ClO₂ [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 20℃; for 12h;	In a 250 mL flask, add 3.0 g of 2- (3-oxo-2-pentylcyclopentyl) acetic acid, 3.0 g of oxalyl chloride, 150 mL of dichloromethane, DMF (N, N-dimethylformamide) three drops. The reaction was stirred at room temperature for 12 hours. After the reaction is complete, Desolvate under reduced pressure, Add 150 mL of ethyl acetate, 1.5 grams of p-toluidine, Triethylamine 2.0g. The reaction was stirred at room temperature for 2 hours. After TLC monitors the reaction, Wash with 50mL × 3 of water, The organic phase was dried over anhydrous sodium sulfate for 12 hours. Desolvate under reduced pressure, Column chromatography (eluent: ethyl acetate and petroleum ether (boiling range: 60-90 C), The volume ratio is 1: 6) 2- (3-oxo-2-pentylcyclopentyl) acetyl (2,4-dimethoxy) aniline 2.3 g, grey solid.

Reference： [1]Patent: CN110402926,2019,A .Location in patent: Paragraph 0010-0012

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P422
P402 + P404	Store in a dry place. Store in a closed container.
P403 + P233	Store in a well-ventilated place. Keep container tightly closed.
P403 + P235	Store in a well-ventilated place. Keep cool.
P410 + P403	Protect from sunlight. Store in a well-ventilated place.
P410 + P412	Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF.
P411 + P235	Keep cool.
Disposal
Code	Phrase
P501	Dispose of contents/container to ...
P502	Refer to manufacturer/supplier for information on recovery/recycling

Purity	Size	Price	VIP Price	USA Stock *0-1 Day	Global Stock *5-7 Days	Quantity
{[ item.p_purity ]}	{[ item.pr_size ]}	{[ getRatePrice(item.pr_usd, 1,1) ]} {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate) ]}	{[ getRatePrice(item.pr_usd, 1,1) ]}	Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate) ]} {[ getRatePrice(item.pr_usd,1,item.mem_rate) ]}	{[ item.pr_usastock ]}	Inquiry -	{[ item.pr_chinastock ]}	Inquiry -

Physical hazards
Code	Phrase
H200	Unstable explosive
H201	Explosive; mass explosion hazard
H202	Explosive; severe projection hazard
H203	Explosive; fire, blast or projection hazard
H204	Fire or projection hazard
H205	May mass explode in fire
H220	Extremely flammable gas
H221	Flammable gas
H222	Extremely flammable aerosol
H223	Flammable aerosol
H224	Extremely flammable liquid and vapour
H225	Highly flammable liquid and vapour
H226	Flammable liquid and vapour
H227	Combustible liquid
H228	Flammable solid
H229	Pressurized container: may burst if heated
H230	May react explosively even in the absence of air
H231	May react explosively even in the absence of air at elevated pressure and/or temperature
H240	Heating may cause an explosion
H241	Heating may cause a fire or explosion
H242	Heating may cause a fire
H250	Catches fire spontaneously if exposed to air
H251	Self-heating; may catch fire
H252	Self-heating in large quantities; may catch fire
H260	In contact with water releases flammable gases which may ignite spontaneously
H261	In contact with water releases flammable gas
H270	May cause or intensify fire; oxidizer
H271	May cause fire or explosion; strong oxidizer
H272	May intensify fire; oxidizer
H280	Contains gas under pressure; may explode if heated
H281	Contains refrigerated gas; may cause cryogenic burns or injury
H290	May be corrosive to metals
Health hazards
Code	Phrase
H300	Fatal if swallowed
H301	Toxic if swallowed
H302	Harmful if swallowed
H303	May be harmful if swallowed
H304	May be fatal if swallowed and enters airways
H305	May be harmful if swallowed and enters airways
H310	Fatal in contact with skin
H311	Toxic in contact with skin
H312	Harmful in contact with skin
H313	May be harmful in contact with skin
H314	Causes severe skin burns and eye damage
H315	Causes skin irritation
H316	Causes mild skin irritation
H317	May cause an allergic skin reaction
H318	Causes serious eye damage
H319	Causes serious eye irritation
H320	Causes eye irritation
H330	Fatal if inhaled
H331	Toxic if inhaled
H332	Harmful if inhaled
H333	May be harmful if inhaled
H334	May cause allergy or asthma symptoms or breathing difficulties if inhaled
H335	May cause respiratory irritation
H336	May cause drowsiness or dizziness
H340	May cause genetic defects
H341	Suspected of causing genetic defects
H350	May cause cancer
H351	Suspected of causing cancer
H360	May damage fertility or the unborn child
H361	Suspected of damaging fertility or the unborn child
H361d	Suspected of damaging the unborn child
H362	May cause harm to breast-fed children
H370	Causes damage to organs
H371	May cause damage to organs
H372	Causes damage to organs through prolonged or repeated exposure
H373	May cause damage to organs through prolonged or repeated exposure
Environmental hazards
Code	Phrase
H400	Very toxic to aquatic life
H401	Toxic to aquatic life
H402	Harmful to aquatic life
H410	Very toxic to aquatic life with long-lasting effects
H411	Toxic to aquatic life with long-lasting effects
H412	Harmful to aquatic life with long-lasting effects
H413	May cause long-lasting harmful effects to aquatic life
H420	Harms public health and the environment by destroying ozone in the upper atmosphere

[ CAS No. 3572-64-3 ] {[proInfo.proName]}

Quality Control of [ 3572-64-3 ]

Related Doc. of [ 3572-64-3 ]

Product Details of [ 3572-64-3 ]

Calculated chemistry of [ 3572-64-3 ]

Physicochemical Properties

Pharmacokinetics

Lipophilicity

Druglikeness

Water Solubility

Medicinal Chemistry

Safety of [ 3572-64-3 ]

Application In Synthesis of [ 3572-64-3 ]

[ 3572-64-3 ] Synthesis Path-Upstream 1~2

[ 3572-64-3 ] Synthesis Path-Downstream 1~24

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

Inquiry