[ CAS No. 215162-34-8 ] {[proInfo.proName]}

Name: 215162-34-8|2,2',2''-(Benzene-1,3,5-triyltris(oxy))triacetic acid|95%
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Quality Control of [ 215162-34-8 ]

COA NMR CNMR HPLC LC-MS

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Product Details of [ 215162-34-8 ]

CAS No. :	215162-34-8	MDL No. :	MFCD17012727
Formula :	C₁₂H₁₂O₉	Boiling Point :	-
Linear Structure Formula :	-	InChI Key :	OMPLWOKOQNOVCD-UHFFFAOYSA-N
M.W :	300.22	Pubchem ID :	10828045
Synonyms :

Safety of [ 215162-34-8 ]

Signal Word:	Warning	Class:
Precautionary Statements:	P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501	UN#:
Hazard Statements:	H315-H319-H335	Packing Group:
GHS Pictogram:

Application In Synthesis of [ 215162-34-8 ]

* 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.

Downstream synthetic route of [ 215162-34-8 ]

[ 215162-34-8 ] Synthesis Path-Downstream 1~16

1
[ CAS Unavailable ]
[ 215162-34-8 ]
[ 215161-32-3 ]

Yield	Reaction Conditions	Operation in experiment
89%	With N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate In chloroform; N,N-dimethyl-formamide at 25℃; for 16h;

Reference： [1]Boger, Dale L.; Goldberg, Joel; Jiang, Weiqin; Chai, Wenying; Ducray, Pierre; Lee, Jae Kyoo; Ozer, Rachel S.; Andersson, Carl-Magnus [Bioorganic and Medicinal Chemistry, 1998, vol. 6, # 8, p. 1347 - 1378]

2
[ 314241-45-7 ]
[ 215162-34-8 ]

Yield	Reaction Conditions	Operation in experiment
95%	With sodium hydroxide at 80℃; for 12h;

Reference： [1]Kovacs-Kulyassa; Herczegh; Sztaricskai; Szabo [Journal of Antibiotics, 2000, vol. 53, # 10, p. 1207 - 1211]

3
[ 478812-59-8 ]
[ 215162-34-8 ]

Yield	Reaction Conditions	Operation in experiment
99%	With sodium hydroxide In water for 24h; Heating;
92%	With Dowex 50 W-X₈; water for 8h; Heating;

Reference： [1]Huang, Wei; Song, Yuming; Wang, Jing; Cao, Guoying; Zheng, Zhuo [Tetrahedron, 2004, vol. 60, # 46 SPEC. ISS., p. 10469 - 10477]
[2]Lu, Jun; Zeng, Qing-dao; Wang, Chen; Zheng, Qi-yu; Wan, Lijun; Bai, Chunli [Journal of Materials Chemistry, 2002, vol. 12, # 10, p. 2856 - 2858]

4
[ 192803-37-5 ]
[ 215162-34-8 ]
[ 616873-79-1 ]

Yield	Reaction Conditions	Operation in experiment
63%	With dmap; dacarbazine In dichloromethane
63%	With dmap; diisopropylcyanamide In dichloromethane; N,N-dimethyl-formamide at 0 - 20℃;

Reference： [1]Song, Yuming; Chen, Huilin; Hu, Xinquan; Bai, Changmin; Zheng, Zhuo [Tetrahedron Letters, 2003, vol. 44, # 37, p. 7081 - 7085]
[2]Huang, Wei; Song, Yuming; Wang, Jing; Cao, Guoying; Zheng, Zhuo [Tetrahedron, 2004, vol. 60, # 46 SPEC. ISS., p. 10469 - 10477]

5
[ 108-73-6 ]
[ 79-11-8 ]
[ 215162-34-8 ]

Yield	Reaction Conditions	Operation in experiment
89%	With sodium hydroxide at 110℃;	1,3,5-Trihydroxybenzene (3.78 g, 0.013 mol), chloroacetic acid (3.4 g, 0.015 mol) and PEG-200 (0.6 g, 0.003 mol) was successively slowly added to 20 mL water containing NaOH (2 g, 0.05 mol) in ice bath. The solution was heated to 110 oC for 5-6 hours, and its pH value was detected during the reaction to keep the reaction system basic. After cooling and filtering, the filtrate was collected and its pH was slowly adjusted to 1 by HCl solution, and solid was precipitated. After filtering the solution and recrystallizing the solid, pure compound 7 was obtained in 89% yield. 2,2',2''-(benzene-1,3,5-triyltris(oxy))triacetic acid (compound 7): 1H NMR (400 MHz, DMSO) δ 6.06 (s, 2H), 4.54 (s, 3H); 13C NMR (100 MHz, DMSO) δ 170.20, 159.57, 94.26, 65.13.
79%	With sodium hydroxide In water at 95 - 100℃; for 0.166667h; Microwave irradiation; Sonication; Green chemistry;	3.2.3. MW-US Method General procedure: In a 50 mL flask, 1mmol of phenol (1-15), the appropriate amount of chloroacetic acid (16) andsodium hydroxide (potassium carbonate for nipagins) and 5 mL of water were mixed.Number of moles of chloroacetic acid (16) and NaOH (K2CO3): 1.2 mmol (0.11 g) of 16 and 2.3 mmol of base for monophenols (1-9) 2.2 mmol (0.21 g) of 16 and 3.3 mmol of base for diphenols (10-12) 3.2 mmol (0.30 g) of 16 and 4.3 mmol of base for triphenols (13-15)A flask with carefully mixed reagents was placed in a MW-US reactor and the contents reactedunder SMUI conditions characterized by the following parameters: MW = 200 W, US = 800 Wat 95-100° C for 10 min. After the process was complete, concentrated hydrochloric acid wasadded to the reaction mixture until an acidic pH~3 was obtained, to isolate the free products. Theseparated precipitate was filtered off. The main product was purified by crystallization or columnchromatography using a mixture of chloroform and methanol (9:1 or 5:1) as an eluent.
55%	Stage #1: chloroacetic acid With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: 3,5-dihydroxyphenol With potassium carbonate In N,N-dimethyl-formamide at 74 - 78℃; for 12h; Further stages.;

Reference： [1]Zhang, Tong; Bai, Cui-Bing; Wu, Yue-Hua; Wang, Nai-Xing; Xu, Bao-Cai; Yan, Zhan; Xing, Yalan [Synthetic Communications, 2019, vol. 49, # 3, p. 410 - 416]
[2]Pawełczyk, Anna; Sowa-Kasprzak, Katarzyna; Olender, Dorota; Zaprutko, Lucjusz [Molecules, 2018, vol. 23, # 9]
[3]Wu, Gang; Wang, Yan; Wang, Xiao-Feng; Kawaguchi, Hiroyuki; Sun, Wei-Yin [Journal of Chemical Crystallography, 2007, vol. 37, # 3, p. 199 - 205]

6
[ 13121-70-5 ]
[ 215162-34-8 ]
[ 1962942-13-7 ]

Yield	Reaction Conditions	Operation in experiment
39.8%	In methanol for 22h; Inert atmosphere; Reflux;	4 Example 4: Preparation of tricyclohexyltin 1,3,5-benzentrioxyacetate: To a 150mL three-necked flask under nitrogen protection was added 1.500g (5.0mmol) 1,3,5-benzenetrioxyacetate, 6.352g (16.5mmol) tricyclohexylstannyl hydroxide, 80mL of anhydrous methanol. It was stirred at reflux for 22h. After completion of the reaction, cooled to room temperature, filtered, and the pressure 0.004MPa, a temperature of 30 under the conditions, and the filtrate was evaporated to dryness with a rotary evaporator to give tricyclohexyltin trimesic oxygen acetate crude products, with dichloromethane - methanol mixed solvent recrystallized from methylene chloride and methanol wherein the volume ratio of 1: 4, at 15 ~ 35 conditions, control crystallization solvent evaporation to give a white solid that is tricyclohexyltin the present invention trimesic oxygen acetate. Yield: 39.8%.

Reference： [1]Current Patent Assignee: HENGYANG NORMAL UNIVERSITY - CN105732696, 2016, A Location in patent: Paragraph 0054; 0055; 0056; 0057; 0058

7
[ CAS Unavailable ]
[ CAS Unavailable ]
[ CAS Unavailable ]
[ 7732-18-5 ]
[ 215162-34-8 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
29.15%	With hydrogenchloride at 20℃; for 4h; Reflux;	Cs8NaH[(SeMo6O21)C6H3O3(CH2CO2)3]2.10H2O(1): TCMB(0.030 g, 0.10 mmol) was dissolved in 9 mL water, then under intensestirring Na2MoO42H2O (0.140 g, 0.60 mmol), SeO2 (0.011 g,0.10 mmol) and CsCl (0.034 g, 0.20 mmol) were added. The pH value ofthe solution was adjusted to 3.9 using 1 mol L1 HCl solution, then themixture was stirred for 2 h under ambient conditions. After another 2 h ofreflux, the mixture was cooled down to room temperature and filtered toa 25 mL beaker. The colorless columnar crystals were acquired after oneweek of standing. Yield: 29.15% (0.056 g) for 1 based onNa2MoO42H2O. Anal. Calcd (%) for 1: Mo 29.97, C 7.50, H 1.02, Found:Mo 31.26, C 7.44, H 1.15. IR (KBr pellet): 3402 (s), 1591 (s), 1459 (m),1430 (m), 1358 (m), 1172 (m), 1151 (m), 1088 (w), 907 (s), 783 (s), 749(s), 667 (s).

Reference： [1]Wang, Jin; Ma, Pengtao; Wang, Yaping; Zhang, Dongdi; Niu, Jingyang; Wang, Jingping [Journal of Physics and Chemistry of Solids, 2017, vol. 110, p. 161 - 166]

8
[ CAS Unavailable ]
[ CAS Unavailable ]
[ 7732-18-5 ]
[ CAS Unavailable ]
[ 215162-34-8 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
39.96%	With hydrogenchloride at 20℃; for 4h; Reflux;	General procedure: TCMB(0.030 g, 0.10 mmol) was dissolved in 9 mL water, then under intensestirring Na2MoO42H2O (0.140 g, 0.60 mmol), SeO2 (0.011 g,0.10 mmol) and CsCl (0.034 g, 0.20 mmol) were added. The pH value ofthe solution was adjusted to 3.9 using 1 mol L1 HCl solution, then themixture was stirred for 2 h under ambient conditions. After another 2 h ofreflux, the mixture was cooled down to room temperature and filtered toa 25 mL beaker. The colorless columnar crystals were acquired after oneweek of standing. Yield: 29.15% (0.056 g) for 1 based onNa2MoO42H2O.

Reference： [1]Wang, Jin; Ma, Pengtao; Wang, Yaping; Zhang, Dongdi; Niu, Jingyang; Wang, Jingping [Journal of Physics and Chemistry of Solids, 2017, vol. 110, p. 161 - 166]

9
[ 771-61-9 ]
[ 215162-34-8 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
82%	With diisopropyl-carbodiimide In tetrahydrofuran at 20℃;	Compound 7 (3.5 g, 0.012 mol), pentafluorophenol (2.6 g, 0.014 mol) and DIC (1.8 g, 0.014 mol) were added in flask with THF as solvent. The reaction was stirred overnight at room temperature and monitored by TLC. After the reaction was finished, the intermediate compound 8 was purified by column chromatography in 82% yield. tris(6,6,6,6,6-pentafluoro-6l8-hexa-1,3,5-triyn-1-yl) 2,2',2''-(benzene-1,3,5-triyltris(oxy))triacetate (compound 8): 1H NMR (400 MHz, CDCl3) δ 6.29 (s, 3H), 4.98 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 164.66, 159.59, 142.39, 141.25, 139.88, 139.30, 136.79, 124.40, 96.25, 64.79; HRMS (ESI) m/z: [M+Na]+ calcd for C30H9F15O9 820.9899; found, 820.9898.

Reference： [1]Zhang, Tong; Bai, Cui-Bing; Wu, Yue-Hua; Wang, Nai-Xing; Xu, Bao-Cai; Yan, Zhan; Xing, Yalan [Synthetic Communications, 2019, vol. 49, # 3, p. 410 - 416]

10
[ 38634-05-8 ]
[ 7732-18-5 ]
[ 5970-45-6 ]
[ 215162-34-8 ]
[Zn2(1,3,5-tris(carboxylatomethoxy)benzene)(4-amino-3,5-bis(4-pyridyl)-1,2,4-triazole)(μ3-OH)]n·nH2O [ No CAS ]

Reference： [1]Crystal Growth and Design,2019,vol. 19,p. 2308 - 2321

11
[ CAS Unavailable ]
[ 7732-18-5 ]
[ 215162-34-8 ]
[ 1135-32-6 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
	In acetonitrile at 140℃; for 72h; Autoclave;	Preparation of [Mn2(HL)2(bpe)(H2O)8]·5H2O}n (1) A mixture of H3L(15 mg, 0.05 mmol), MnCl2·4H2O (9.89,0.05 mmol mg), bpe (9.11 mg, 0.05 mmol), CH3CN(3 mL)and H2O(2 mL) was sealed in a 25-mL Teflon-lined autoclave,heated to 140 °C for 72 h and then cooled to roomtemperature. Yellow block crystals were obtained. Elementalanalysis calcd. (%) for C36H56Mn2N2O31:C 38.51, H 5.03,N 2.50. Found: C 38.49, H 5.09, N 2.55. IR (KBr, cm-1):1575(s), 1474(w), 1407(m), 1330(m), 1164(s), 1064(m),956(w), 808(w), 714(m), 560(w), 539(w).

Reference： [1]Wu, Wei-Li; Dong, Jian-Peng; Liu, Ke-Cheng; Jin, Yu-Jie; Li, Bo; Wang, Li-Ya [Transition Metal Chemistry, 2021, vol. 46, # 1, p. 73 - 79]

12
[ 7732-18-5 ]
[ CAS Unavailable ]
[ 215162-34-8 ]
[ 1135-32-6 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
	In acetonitrile at 130℃; for 72h; Autoclave;	Preparation of [Ni3(L)2(bpe)3(H2O)6]·3H2O}n (2) A mixture of H3L(15 mg, 0.05 mmol), Ni(Ac)3·4H2O(12.46 mg, 0.05 mmol), bpe (9.11 mg, 0.05 mmol), CH3CN(3 mL) and H2O(2 mL) was sealed in a 25-mL Teflonlinedautoclave, heated to 130 °C for 72 h and then cooledat 5 °C/h to room temperature. Green needle crystals wereobtained. Elemental analysis calcd. (%) for C60H66N6Ni3O27:C 48.72, H 4.50, N 5.68. Found: C 48.79, H 4.56, N 5.74. IR(KBr, cm-1): 1605(s), 1415(s), 1319(m), 1258(m), 1154(s),1077(m), 818(m), 705(w).

Reference： [1]Wu, Wei-Li; Dong, Jian-Peng; Liu, Ke-Cheng; Jin, Yu-Jie; Li, Bo; Wang, Li-Ya [Transition Metal Chemistry, 2021, vol. 46, # 1, p. 73 - 79]

13
[ CAS Unavailable ]
[ 7732-18-5 ]
[ 215162-34-8 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
30%	With 1,2,3-Benzotriazole In ethanol at 100℃; for 72h; Sealed tube; Autoclave;	2.2. Preparation and characterization for [Co3 (TCMB)2(H2O)4]n•4nH2O(1)and [Zn3(TCMB)( μ3 -OH)3]n•0.5nH2O (2) For the complex 1 , through mixing the 60 mg and 0.20 mmol Co(NO3)2•6H2O, 15 mg and 0.05 mmol H3TCMB, and 12 mg and 0.1 mmol 1H-Benzotriazole with 4 mL of ethanol and 4 mL of wa- ter, we can gain a mixture, after that, sealed the mixture in the 15 mL reactor lined with Teflon and then heated it for three days at 100 °C. Thus, the pink crystals with sheet-shape were acquired with 30% yield on the basis of the H 3 TCMB. Anal. Calcd for the C 24 H 34 O 26 Co 3 : H, 3.74 and C, 31.49. Found: H, 3.85 and C, 31.22.

Reference： [1]Yuan, Zhi; Lin, Hai; Zhang, Lei; Peng, Yu; Jin, Yuan; Pi, Zhi-Bing; Zhang, Jun-Kai [Journal of Molecular Structure, 2021, vol. 1228]

14
[ CAS Unavailable ]
[ 7732-18-5 ]
[ 215162-34-8 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
44%	With 1,2,3-Benzotriazole; tetrafluoroboric acid In ethanol at 100℃; for 72h; Sealed tube; Autoclave;	For the complex 2 , via mixing the 48 mg and 0.20 mmol Zn(NO3)2•6H2O, 15 mg and 0.05 mmol H3 TCMB, and 12 mg and 0.1 mmol 1H-Benzotriazole, as well as 30 μL of the HBF4 (50% aq) with 4 mL of water and 4 mL of ethanol, we can gain a mix- ture, after that, sealed the mixture in the 15 mL reactor lined with Teflon and then heated it for three days at 100 °C. Thus, the color- less crystals with sheet-shape were acquired with 44% yield. Anal. Calcd for the C 12 H 13 O 12.5 Zn 3 : H, 2.39 and C, 26.31. Found: H, 2.45 and C, 27.23.

Reference： [1]Yuan, Zhi; Lin, Hai; Zhang, Lei; Peng, Yu; Jin, Yuan; Pi, Zhi-Bing; Zhang, Jun-Kai [Journal of Molecular Structure, 2021, vol. 1228]

15
[ 4916-57-8 ]
[ CAS Unavailable ]
[ 7732-18-5 ]
[ 215162-34-8 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
43%	In methanol at 85℃; for 72h;	Preparation and Characterization for[Cu4(TCMB)2(bpee)2(μ3-OH)2(H2O)2]n·12nH2O (1) and[Zn4(TCMB)2(bpee)2(μ3-OH)2(H2O)2]n·12nH2O (2 For the complex 1, through mixing 48 mg and 0.20 mmolCu(NO3)2·3H2O, 15 mg and 0.05 mmol H3TCMB, and18 mg and 0.10 mmol bpee with 4 mL of methanol, and 4mL of water in the 15 mL reactor lined with Teflon to producea mixture, and heated the obtainedmixture for 72 hours at 85 .Thus, we can acquire the blue crystals with rod-shape with43% yield. Anal. Calcd for the C48H68N4O34Cu4: N, 3.74;H,4.57 and C, 38.45. Found: N, 3.98; H, 4.61 and C, 38.45. ICPcalculated for Cu (wt%): C, 38.45; Found: 37.94.

Reference： [1]Zhao, Qin-Ming; Xu, Zhong-You; Zhu, Hui-Peng; He, Yu-Xiang; Wang, Mo [Journal of Fluorescence, 2021, vol. 31, # 3, p. 703 - 712]

16
[ 4916-57-8 ]
[ CAS Unavailable ]
[ 7732-18-5 ]
[ 215162-34-8 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
43%	In methanol at 85℃; for 72h;	For the complex 2, through mixing 48 mg and 0.20 mmolZn(NO3)2·6H2O, 15 mg and 0.05mmol H3TCMB, 18mg and0.10 mmol bpee and 30 μL of HBF4 (50% aq) with 4 mL ofethanol, and 4 mL of water in the 15 mL reactor lined withTeflon to produce a mixture, and heated the obtained mixturefor three days at 85 . Thus, we can acquire the colorless crystalswith sheet-shape with 44% yield. Anal. Calcd for theC48H68N4O34Zn4: N, 3.72; H, 4.55 and C, 38.27. Found: N,3.87; H, 4.49 and C, 38.11. ICP calculated for Zn (wt%): C,17.36; Found: 17.68.

Reference： [1]Zhao, Qin-Ming; Xu, Zhong-You; Zhu, Hui-Peng; He, Yu-Xiang; Wang, Mo [Journal of Fluorescence, 2021, vol. 31, # 3, p. 703 - 712]

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P412	Do not expose to temperatures exceeding 50 oC/ 122 oF.
P413
P420	Store away from other materials.
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. 215162-34-8 ] {[proInfo.proName]}

Quality Control of [ 215162-34-8 ]

Related Doc. of [ 215162-34-8 ]

Product Details of [ 215162-34-8 ]

Safety of [ 215162-34-8 ]

Application In Synthesis of [ 215162-34-8 ]

[ 215162-34-8 ] Synthesis Path-Downstream 1~16

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

Inquiry