CAS 132715-69-6

2-Bromo-3-fluorobenzoic acid

Description:

2-Bromo-3-fluorobenzoic acid is an aromatic carboxylic acid characterized by the presence of both bromine and fluorine substituents on the benzene ring. Specifically, the bromine atom is located at the second position and the fluorine atom at the third position relative to the carboxylic acid group. This compound typically appears as a white to off-white solid and is soluble in organic solvents. Its molecular structure contributes to its unique chemical properties, including its reactivity in electrophilic aromatic substitution reactions and potential applications in pharmaceuticals and agrochemicals. The presence of halogen atoms can influence the acidity of the carboxylic group, as well as the compound's overall polarity and lipophilicity. Additionally, 2-Bromo-3-fluorobenzoic acid can serve as an important intermediate in organic synthesis, facilitating the introduction of various functional groups. Safety data should be consulted for handling and storage, as halogenated compounds can exhibit toxicity and environmental concerns.

Formula: C₇H₄BrFO₂

InChI: InChI=1/C7H4BrFO2/c8-6-4(7(10)11)2-1-3-5(6)9/h1-3H,(H,10,11)

SMILES: c1cc(c(c(c1)F)Br)C(=O)O

Synonyms:

• 3-Fluoro-2-bromobenzoic acid

2-Bromo-3-fluorobenzoic Acid

CAS: 132715-69-6

Formula: C₇H₄BrFO₂

Purity: >96.0%(GC)(T)

Color and Shape: White to Light yellow to Light orange powder to crystal

Molecular weight: 219.01

Ref: 3B-B3722

Benzoic acid, 2-bromo-3-fluoro-

CAS: 132715-69-6

Formula: C₇H₄BrFO₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 219.0079

Ref: IN-DA00111K

2-Bromo-3-fluorobenzoic acid

CAS: 132715-69-6

2-Bromo-3-fluorobenzoic acid

Formula: C₇H₄BrFO₂

Purity: 98%

Color and Shape: white solid

Molecular weight: 219.01g/mol

Ref: 54-PC3917

2-Bromo-3-fluorobenzoic acid

CAS: 132715-69-6

2-Bromo-3-fluorobenzoic acid is a chemical compound that can be synthesized by the reduction of nitrobenzene with ammonium chloride. This reaction is regioselective, giving predominantly 2-bromo-3-fluorobenzoic acid. The reaction proceeds via a nucleophilic substitution mechanism and the product is formed in high yield. A second route for the synthesis of 2-bromo-3-fluorobenzoic acid involves the deamination of trifluorotoluene to produce hypophosphorous acid, which reacts with sulfuric acid to give 2-bromo-3-fluorobenzoic acid. The bromine atom in this molecule has a high nucleophilicity and reacts readily with electrophiles such as ammonia and amines.

Formula: C₇H₄BrFO₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 219.01 g/mol

Ref: 3D-FB38482

2-Bromo-3-fluorobenzoic acid

CAS: 132715-69-6

Formula: C₇H₄BrFO₂

Purity: 96%

Color and Shape: Very pale yellow to pale reddish yellow powder

Molecular weight: 219.009

Ref: 10-F005469