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2-bromo-5-cyanobenzoic acid

CAS No.
845616-12-8
Chemical Name:
2-bromo-5-cyanobenzoic acid
Synonyms
2-bromo-5-cyanobenzoic acid;2-bromo-5-cyanobenozic acid;BENZOIC ACID, 2-BROMO-5-CYANO-
CBNumber:
CB71557735
Molecular Formula:
C8H4BrNO2
Molecular Weight:
226.03
MDL Number:
MFCD11847005
MOL File:
845616-12-8.mol
MSDS File:
SDS
Last updated:2026-05-28 03:19:17

2-bromo-5-cyanobenzoic acid Properties

Melting point 183-185°
storage temp. Sealed in dry,Room Temperature
form powder
color yellow

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
HS Code  2916399090

2-bromo-5-cyanobenzoic acid price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth VIB61612 2-Bromo-5-cyanobenzoic acid 845616-12-8 0.5g $365.8 2026-06-05 Buy
Biosynth VIB61612 2-Bromo-5-cyanobenzoic acid 845616-12-8 5g $1357 2026-06-05 Buy
Apolloscientific OR400316 2-Bromo-5-cyanobenzoic acid ≥95% 845616-12-8 100mg $41 2026-06-04 Buy
Apolloscientific OR400316 2-Bromo-5-cyanobenzoic acid ≥95% 845616-12-8 250mg $82 2026-06-04 Buy
Activate Scientific AS41929 2-Bromo-5-cyanobenzoic acid 97% 845616-12-8 1g $203 2026-06-04 Buy
Product number Packaging Price Buy
VIB61612 0.5g $365.8 Buy
VIB61612 5g $1357 Buy
OR400316 100mg $41 Buy
OR400316 250mg $82 Buy
AS41929 1g $203 Buy

2-bromo-5-cyanobenzoic acid Chemical Properties, Uses, Production

Synthesis

2-aMino-5-cyanobenzoic acid

99767-45-0

2-bromo-5-cyanobenzoic acid

845616-12-8

The general procedure for the synthesis of 2-bromo-5-cyanobenzoic acid from 2-amino-5-cyanobenzoic acid was as follows: tert-butyl nitrite (1.15 ml, 8.63 mmol) was added dropwise over 2 min at 0 °C to a suspension of copper (II) bromide (1.6 g, 7.1 mmol) in acetonitrile (30 ml). Subsequently, 2-amino-5-cyanobenzoic acid (1.0 g, 6.17 mmol) was added in batches over 10 min at 0 °C. The reaction mixture was stirred at 0 °C for 2 h, then brought to room temperature and stirred overnight. After completion of the reaction, half of the solvent was evaporated under reduced pressure. The residue was dissolved in a mixture of 1N HCl (15 ml) and ethyl acetate (30 ml). The organic layer was extracted with 1N NaOH (3 x 10 ml). The aqueous layer was acidified with 2N HCl and a solid was precipitated. The solid was collected by filtration, washed with water and dried under high vacuum at 50°C to give 2-bromo-5-cyanobenzoic acid (0.92 g, 66% yield) as a yellow solid.

References

[1] Patent: WO2005/23260, 2005, A1. Location in patent: Page/Page column 48
[2] Patent: US2005/209241, 2005, A1. Location in patent: Page/Page column 20

2-bromo-5-cyanobenzoic acid Preparation Products And Raw materials

Global Suppliers ( 63)
Supplier Tel Email Country ProdList Advantage
shanghai aokchem co., ltd 021-68712331 39130253 aokchem@gmail.com China 332 58
ShangHai AmK Pharmaceutical Technology Co., Ltd. 微信 18019252918 18019252918 sale@amkchem.com China 14982 55
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Capot Chemical Co.,Ltd. +86-(0)57185586718 +86-13336195806 sales@capot.com China 29626 60
2-bromo-5-cyanobenzoic acid BENZOIC ACID, 2-BROMO-5-CYANO- 2-bromo-5-cyanobenozic acid 845616-12-8