276677-03-3

Basic information

• Product Name: 4-Bromo-2,5-dimethylbenzoic acid
• Synonyms: 4-Bromo-2,5-dimethylbenzoic acid
• CAS NO: 276677-03-3
• Molecular Formula: C₉H₉BrO₂
• Molecular Weight: 229.07056
• EINECS: -0
• Mol File: 276677-03-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 171.5-172.5 °C
• Boiling Point: 321.2±30.0 °C(Predicted)
• Appearance: /
• Density: 1.520±0.06 g/cm3(Predicted)
• PKA: 3.69±0.25(Predicted)
• CAS DataBase Reference: 4-Bromo-2,5-dimethylbenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Bromo-2,5-dimethylbenzoic acid(276677-03-3)
• EPA Substance Registry System: 4-Bromo-2,5-dimethylbenzoic acid(276677-03-3)

Safety Data

• Hazardous Substances Data: 276677-03-3(Hazardous Substances Data)

Upstream product

• 110-05-4 di-tert-butyl peroxide 
• 7697-28-1 4-bromo-3-methylbenzoic acid 
• 1074-24-4 2,5-dibromo-p-xylene 
• 95-63-6 1,2,4-Trimethylbenzene 
• 88111-74-4 bromo-4 dimethyl-2,5 benzaldehyde 
• 5469-19-2 1-bromo-2,4,5-trimethylbenzene 
• 7697-37-2 nitric acid 
• 292037-85-5 4-bromo-2,5-dimethylbenzonitrile 
• 108480-48-4 4-bromo-2,5-dimethylbenzyl chloride 
• 824-45-3 2,5-dimethylbenzyl chloride 

Downstream Products

• 276677-04-4 4-bromo-2-ethoxycarbonylmethyl-5-methyl-benzoic acid 
• 276678-65-0 4-bromo-2.5-dimethylbenzoic acid chloride 
• 854663-04-0 3-bromo-1,4-dimethyl-2,5-dinitro-benzene 
• 856352-10-8 2-bromo-3,6-dimethyl-aniline 
• 52415-02-8 2-bromo-1,4-dimethyl-3-nitro-benzene 
• 26829-89-0 2,4-dibromo-3,6-dimethylaniline 
• 858489-42-6 4-bromo-2,5-dimethyl-3,6-dinitro-benzoic acid 

Relevant articles and documents

Preparation method for o-tolylacetic acid aryl formic acid derivative

The invention discloses a preparation method for an o-tolylacetic acid aryl formic acid derivative. According to the method, new C-C bonds can be formed, the organic o-tolylacetic acid aryl formic acid derivative is obtained, the good functional group tolerance is achieved, and the o-tolylacetic acid aryl formic acid derivative which cannot be easily obtained by adopting other methods can be synthesized; according to the method, adopted raw materials are easy to obtain, the yield is high, the reaction conditions are mild, the substrate range is wide, and after-treatment is simple and green.

Substituted aryl and heteroaryl derivatives, their production and their use as medicines

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