ChemicalBook--->CAS DataBase List--->174265-12-4

174265-12-4

174265-12-4 Structure

174265-12-4 Structure
IdentificationBack Directory
[Name]

2-Bromo-5-chlorobenzaldehyde
[CAS]

174265-12-4
[Synonyms]

2-Bromo-5-chlorobenzalde
2-Bromo-5-chlorobenzaldehyde
5-Chloro-2-bromobenzaldehyde
[EINECS(EC#)]

1592732-453-0
[Molecular Formula]

C7H4BrClO
[MDL Number]

MFCD00462870
[MOL File]

174265-12-4.mol
[Molecular Weight]

219.46
Chemical PropertiesBack Directory
[Melting point ]

66 °C
[Boiling point ]

258 °C
[density ]

1.698
[Fp ]

110 °C
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

soluble in Methanol
[form ]

Crystalline
[color ]

Pale yellow
[InChI]

InChI=1S/C7H4BrClO/c8-7-2-1-6(9)3-5(7)4-10/h1-4H
[InChIKey]

IIISHLMCTDMUHH-UHFFFAOYSA-N
[SMILES]

C(=O)C1=CC(Cl)=CC=C1Br
[CAS DataBase Reference]

174265-12-4
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H335-H315-H319
[Precautionary statements ]

P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22
[Safety Statements ]

24/25
[RIDADR ]

UN1993
[HS Code ]

29130000
Hazard InformationBack Directory
[Uses]

2-Bromo-5-chlorobenzaldehyde is an important class of pharmaceutical intermediates which can be used in the synthesis of a variety of drugs. 2-Bromo-5-chlorobenzaldehyde can be used in the preparation of the compound 3-chloro-14-cyclohexyl-6-[2-(dimethylamino)ethyl]-7-oxo-5,6,7,8-tetrahydroindolo[2,1-a][2,5]benzo[di-acridine]-11-carboxylic acid, which can be used in the treatment or prevention of viral infections.
[Synthesis]

2-Bromo-1-bromomethyl-5-chlorobenzene

66192-24-3

2-Bromo-5-chlorobenzaldehyde

174265-12-4

Step 2: Synthesis of 2-bromo-5-chlorobenzaldehyde; Preparation was carried out with reference to the literature method (J. Am. Chem. Soc. 2002, 124(7), 1354): a mixture of activated powdered 4A molecular sieves (800 mg/mmol of substrate), N-methylmorpholine-N-oxide (2 eq.) and 2-bromomethyl-5-chlorobenzaldehyde (1 eq.) was stirred for 2 hours at 0°C in a N -methylpyrrolidone (0.16 M) were stirred for 2 hours. Upon completion of the reaction, the reaction mixture was filtered through a diatomaceous earth pad and the filtrate was subsequently concentrated under vacuum to afford the target product 2-bromo-5-chlorobenzaldehyde in 92% yield.

[References]

[1] Patent: WO2006/46030, 2006, A2. Location in patent: Page/Page column 28
[2] Journal of the American Chemical Society, 2002, vol. 124, # 7, p. 1354 - 1363
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