[ CAS No. 276866-90-1 ]

Name: 4-Chloro-3-iodobenzaldehyde
Brand: Ambeed
SKU: A167203
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Quality Control of [ 276866-90-1 ]

COA NMR CNMR HPLC LC-MS

Related Doc. of [ 276866-90-1 ]

SDS

Product Details of [ 276866-90-1 ]

CAS No. :	276866-90-1	MDL No. :	MFCD09836681
Formula :	C₇H₄ClIO	Boiling Point :	304°C at 760 mmHg
Linear Structure Formula :	-	InChI Key :	ARCZAXXTPLCEMP-UHFFFAOYSA-N
M.W :	266.46	Pubchem ID :	11230916
Synonyms :

Computed Properties of [ 276866-90-1 ]

TPSA :Topological Polar Surface Area	17.1	H-Bond Acceptor Count :	1
XLogP3 :	-	H-Bond Donor Count :	0
SP3 :	0.00	Rotatable Bond Count :	1

Safety of [ 276866-90-1 ]

Signal Word:	Warning	Class	N/A
Precautionary Statements:	P280-P305+P351+P338	UN#:	N/A
Hazard Statements:	H302	Packing Group:	N/A
GHS Pictogram:

Application In Synthesis of [ 276866-90-1 ]

Upstream synthesis route of [ 276866-90-1 ]
Downstream synthetic route of [ 276866-90-1 ]

[ 276866-90-1 ] Synthesis Path-Upstream 1~3

1
[ 104-88-1 ]
[ 276866-90-1 ]

Yield	Reaction Conditions	Operation in experiment
40%	at 20℃; for 1.50 h;	Iodines (1.12 g, 4.4 mmol), and sodium iodates (400mg, 2.2 mmol) are put into the reaction container in which the sulfuric acid (30 ml) is contained and it 30 min.is stirred in at a room temperature. Thereafter, 4- chlorobenzaldehydes (1.40 g, 10.0 mmol) are additionally put and it is stirred in at a room temperature for 1 hour.The reaction mixture is poured into the iced water after the reaction completion and the then generated solidis filtered and until the product is neutralized it washeswith water. After the solid filtered was melted in ethanol it recrystallized and intended compound 1.06 gs (4.00 mmol, 40percent) were obtained.

Reference： [1] Bulletin of the Chemical Society of Japan, 2000, vol. 73, # 4, p. 951 - 956
[2] Tetrahedron, 2004, vol. 60, # 41, p. 9113 - 9119
[3] Synthesis, 2006, # 7, p. 1195 - 1199
[4] Patent: KR2016/149561, 2016, A. Location in patent: Paragraph 0125; 0126; 0127
[5] European Journal of Medicinal Chemistry, 2016, vol. 123, p. 180 - 190

2
[ 104317-95-5 ]
[ 276866-90-1 ]

Reference： [1] Patent: WO2006/125511, 2006, A1. Location in patent: Page/Page column 56-57

3
[ 16588-34-4 ]
[ 276866-90-1 ]

Reference： [1] Journal of the Chemical Society, 1927, p. 25

[ 276866-90-1 ] Synthesis Path-Downstream 1~10

1
[ 104-88-1 ]
[ 276866-90-1 ]

Yield	Reaction Conditions	Operation in experiment
40%	With sodium iodate; sulfuric acid; at 20℃; for 1.5h;	Iodines (1.12 g, 4.4 mmol), and sodium iodates (400mg, 2.2 mmol) are put into the reaction container in which the sulfuric acid (30 ml) is contained and it 30 min.is stirred in at a room temperature. Thereafter, 4- chlorobenzaldehydes (1.40 g, 10.0 mmol) are additionally put and it is stirred in at a room temperature for 1 hour.The reaction mixture is poured into the iced water after the reaction completion and the then generated solidis filtered and until the product is neutralized it washeswith water. After the solid filtered was melted in ethanol it recrystallized and intended compound 1.06 gs (4.00 mmol, 40%) were obtained.

Reference： [1]Bulletin of the Chemical Society of Japan,2000,vol. 73,p. 951 - 956
[2]Tetrahedron,2004,vol. 60,p. 9113 - 9119
[3]Synthesis,2006,p. 1195 - 1199
[4]Patent: KR2016/149561,2016,A.Location in patent: Paragraph 0125; 0126; 0127
[5]European Journal of Medicinal Chemistry,2016,vol. 123,p. 180 - 190

2
[ 16588-34-4 ]
[ 276866-90-1 ]

Reference： [1]Journal of the Chemical Society,1927,p. 25

3
[ 276866-90-1 ]
1-(6-chloro-2'-methoxy-[1,1'-biphenyl]-3-yl)-N-methyl methane amide [ No CAS ]

Reference： [1]European Journal of Medicinal Chemistry,2016,vol. 123,p. 180 - 190

4
[ 276866-90-1 ]
1-(6-chloro-2'-methoxy-[1,1'-biphenyl]-3-yl)-N,N-dimethylmethanamine [ No CAS ]

Reference： [1]European Journal of Medicinal Chemistry,2016,vol. 123,p. 180 - 190

5
[ 276866-90-1 ]
1-((6-chloro-2'-methoxy-[1,1'-biphenyl]-3-yl)methyl)-4-methylpiperidine [ No CAS ]

Reference： [1]European Journal of Medicinal Chemistry,2016,vol. 123,p. 180 - 190

6
[ 276866-90-1 ]
1-((6-chloro-2'-methoxy-[1,1'-biphenyl]-3-yl)methyl)-4-(2-methoxyphenyl)piperazine [ No CAS ]

Reference： [1]European Journal of Medicinal Chemistry,2016,vol. 123,p. 180 - 190

7
[ 5720-06-9 ]
[ 276866-90-1 ]
6-chloro-2'-methoxy-[1,1'-biphenyl]-3-carbaldehyde [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
64%	With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In N,N-dimethyl-formamide; at 150℃;Inert atmosphere;	General procedure: 2-Methoxyphenylboronic acid 6 (1.2mmol), Pd(PPh3)4 (0.1mmol) and Na2CO3 (1.5mmol) were added to a solution of benzaldehyde 5 (1.0mmol) in DMF (20ml). The mixture was stirred for overnight at 150 C. After cooling down to room temperature, the reaction mixture was quenched with saturated NaHCO3 and then extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered, and evaporated. The residue was purified by column chromatography on silica gel (Hexane:Ether=10:1) to obtain desired product 7 in 64-98% yields.<LineBreak />5.1.1.1 6-Chloro-2'-methoxy-[1,1'-biphenyl]-3-carbaldehyde (7b) 64% Yield (as a white solid): mp 82-83 C; 1H NMR (400 MHz, CDCl3) delta 9.99 (s, CHO), 7.81-7.78 (m, 2ArH), 7.61 (d, J = 8.8 Hz, ArH), 7.43-7.39 (m, ArH), 7.20 (dd, J = 7.6, 2.0 Hz, ArH), 7.04 (td, J = 7.6, 0.8 Hz, ArH), 7.00 (d, J = 8.4 Hz, ArH), 3.78 (s, OCH3); 13C NMR (CDCl3, 100 MHz) delta 191.09, 156.64, 140.80, 138.90, 134.75, 133.30, 130.79, 130.25, 130.01, 129.01, 127.21, 120.54, 111.04, 55.58; HRMS (ESI+) calcd for C14H11ClNaO2+ [M + Na]+ 269.0340, found 269.0343.
	With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In N,N-dimethyl-formamide; at 160℃; for 6.0h;	To the reaction vessel were added <strong>[276866-90-1]4-chloro-3-iodobenzaldehyde</strong> (3.81 mmol), 2-methoxyphenylboronic acid (4.58 mmol), Pd (PPh3) 4 (0.038 mmol) and sodium carbonate (5.72 mmol) -dimethylformamide (20 ml) at 160 & lt; 0 & gt; C The mixture was heated to reflux for 6 hours. After completion of the reaction, the reaction mixture was diluted with ethyl acetate, and then saturated sodium hydrogencarbonate The organic layer obtained by extracting the aqueous layer with ethyl acetate was dried over anhydrous MgSO 4 and filtered. Filtrate The concentrate was separated and purified by column chromatography (hexane: ethyl acetate = 2: 1) to obtain the desired compound .

Reference： [1]European Journal of Medicinal Chemistry,2016,vol. 123,p. 180 - 190
[2]Patent: KR2016/149561,2016,A.Location in patent: Paragraph 0129

8
[ 104317-95-5 ]
[ 276866-90-1 ]

Reference： [1]Patent: WO2006/125511,2006,A1.Location in patent: Page/Page column 56-57

9
[ 276866-90-1 ]
[ 107-21-1 ]
[ 915944-55-7 ]

Reference： [1]Patent: WO2006/125511,2006,A1.Location in patent: Page/Page column 57

10
[ 276866-90-1 ]
[ 914105-93-4 ]

Reference： [1]Journal of Medicinal Chemistry,2007,vol. 50,p. 2468 - 2485

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P235 + P410	Keep cool. Protect from sunlight.
Response
Code	Phrase
P301	IF SWALLOWED:
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P320
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P321
P322
P330	Rinse mouth.
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P342	If experiencing respiratory symptoms:
P350	Gently wash with plenty of soap and water.
P351	Rinse cautiously with water for several minutes.
P352	Wash with plenty of soap and water.
P353	Rinse skin with water/shower.
P360	Rinse immediately contaminated clothing and skin with plenty of water before removing clothes.
P361	Remove/Take off immediately all contaminated clothing.
P362	Take off contaminated clothing and wash before reuse.
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P370	In case of fire:
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P376	Stop leak if safe to do so. Oxidising gases (section 2.4) 1
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P378
P380	Evacuate area.
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P390	Absorb spillage to prevent material damage.
P391	Collect spillage. Hazardous to the aquatic environment
P301 + P310	IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
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P301 + P330 + P331	IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P302 + P334	IF ON SKIN: Immerse in cool water/wrap in wet bandages.
P302 + P350	IF ON SKIN: Gently wash with plenty of soap and water.
P303 + P361 + P353	IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P304 + P312	IF INHALED: Call a POISON CENTER or doctor/physician if you feel unwell.
P304 + P340	IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P304 + P341	IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P305 + P351 + P338	IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P306 + P360	IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes.
P307 + P311	IF exposed: call a POISON CENTER or doctor/physician.
P308 + P313	IF exposed or concerned: Get medical advice/attention.
P309 + P311	IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician.
P332 + P313	IF SKIN irritation occurs: Get medical advice/attention.
P333 + P313	IF SKIN irritation or rash occurs: Get medical advice/attention.
P335 + P334	Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages.
P337 + P313	IF eye irritation persists: Get medical advice/attention.
P342 + P311	IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician.
P370 + P376	In case of fire: Stop leak if safe to Do so.
P370 + P378	In case of fire:
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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
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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
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H271	May cause fire or explosion; strong oxidizer
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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. 276866-90-1 ]

Quality Control of [ 276866-90-1 ]

Related Doc. of [ 276866-90-1 ]

Product Details of [ 276866-90-1 ]

Computed Properties of [ 276866-90-1 ]

Safety of [ 276866-90-1 ]

Application In Synthesis of [ 276866-90-1 ]

[ 276866-90-1 ] Synthesis Path-Upstream 1~3

[ 276866-90-1 ] Synthesis Path-Downstream 1~10

Related Functional Groups of [ 276866-90-1 ]

Aryls

Chlorides

Aldehydes

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

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Related Functional Groups of
[ 276866-90-1 ]