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ChemicalBook--->CAS DataBase List--->158435-41-7

158435-41-7

158435-41-7 Structure

158435-41-7 Structure
IdentificationMore
[Name]

2-Chloro-4-bromobenzaldehyde
[CAS]

158435-41-7
[Synonyms]

4-BROMO-2-CHLOROBENZALDEHYDE
2-Chloro-4-bromobenzaldehyde
[Molecular Formula]

C7H4BrClO
[MDL Number]

MFCD08741413
[Molecular Weight]

219.46
[MOL File]

158435-41-7.mol
Chemical PropertiesBack Directory
[Melting point ]

74-76℃
[Boiling point ]

271.3±25.0 °C(Predicted)
[density ]

1.698±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[color ]

White to Orange to Green
[Sensitive ]

Air Sensitive
[CAS DataBase Reference]

158435-41-7(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

C
[Risk Statements ]

22
[Hazard Note ]

Corrosive
[HS Code ]

2913000090
Hazard InformationBack Directory
[Chemical Properties]

Light yellow crystalline powder
[Uses]

4-Bromo-2-chlorobenzaldehyde is a useful research chemical for organic synthesis and other chemical processes.4-Bromo-2-chlorobenzaldehyde is used in preparation of Heterocyclic compounds as P2X3 antagonist and its intermediate.
[Synthesis]

(4-Bromo-2-chlorophenyl)methanol

185315-48-4

2-Chloro-4-bromobenzaldehyde

158435-41-7

General procedure for the synthesis of 2-chloro-4-bromobenzaldehyde from (4-bromo-2-chlorophenyl)methanol: Oxalyl chloride (6.9 g, 54 mmol, 1.3 eq.) was dissolved in dichloromethane (DCM, 153 mL) and the solution was cooled to -78 °C. A solution of DCM (57 mL) in dimethyl sulfoxide (DMSO, 4.72 mL, 66.5 mmol, 1.6 eq.) was slowly added dropwise to the cooled solution at -78 °C and stirred for 15 min. (4-Bromo-2-chlorophenyl)methanol (Compound 43, 9.2 g, 41.5 mmol, 1.0 eq.) was dissolved in DCM (116 mL) and added drop-wise to the above cooled solution, keeping the temperature at -78 °C. Stirring was continued at -78 °C for 2 hours. Subsequently, triethylamine (TEA, 28.7 mL, 207 mmol, 5 eq.) was added to slowly warm the reaction mixture to room temperature. After stirring for 30 min at room temperature, the reaction mixture was diluted with DCM (300 mL), washed sequentially with saturated ammonium chloride (NH4Cl) solution and brine, dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated in vacuum to afford 2-chloro-4-bromobenzaldehyde (Compound 44) in 96% yield (8.8 g).

[References]

[1] Patent: WO2008/51826, 2008, A2. Location in patent: Page/Page column 53; 54
[2] Patent: WO2008/103277, 2008, A2. Location in patent: Page/Page column 197
[3] Journal of Medicinal Chemistry, 2017, vol. 60, # 18, p. 7820 - 7834
[4] Patent: WO2013/75083, 2013, A1. Location in patent: Paragraph 006309; 00632
[5] Patent: US9206128, 2015, B2. Location in patent: Page/Page column 275; 276; 277
Spectrum DetailBack Directory
[Spectrum Detail]

2-Chloro-4-bromobenzaldehyde(158435-41-7)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

4-Bromo-2-chlorobenzaldehyde, 95%(158435-41-7)
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