CAS 627531-47-9

4-bromo-3-chloro-2-methylaniline

Description:

4-Bromo-3-chloro-2-methylaniline is an organic compound characterized by its aromatic amine structure, which includes a benzene ring substituted with a bromine atom at the para position, a chlorine atom at the meta position, and a methyl group at the ortho position relative to the amino group. This compound typically appears as a solid and is soluble in organic solvents, reflecting its hydrophobic characteristics due to the presence of halogen substituents. The presence of both bromine and chlorine introduces significant electronegativity, influencing the compound's reactivity and potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The amino group (-NH2) contributes to its basicity and potential for further chemical modifications. Additionally, the compound's structure suggests it may exhibit specific biological activities, making it of interest in medicinal chemistry. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks.

Formula: C₇H₇BrClN

InChI: InChI=1/C7H7BrClN/c1-4-6(10)3-2-5(8)7(4)9/h2-3H,10H2,1H3

SMILES: Cc1c(ccc(c1Cl)Br)N

Synonyms:

• Benzenamine, 4-bromo-3-chloro-2-methyl-
• 4-BROMO-3-CHLORO-2-METHYLANILINE

4-Bromo-3-chloro-2-methylaniline

CAS: 627531-47-9

Formula: C₇H₇BrClN

Purity: 97%

Color and Shape: Solid

Molecular weight: 220.4942

Ref: IN-DA00366B

4-Bromo-3-chloro-2-methylaniline

CAS: 627531-47-9

4-Bromo-3-chloro-2-methylaniline

Formula: C₇H₇BrClN

Purity: 96%

Color and Shape: dark brown solid

Molecular weight: 220.49g/mol

Ref: 54-OR11564

4-Bromo-3-chloro-2-methylaniline

CAS: 627531-47-9

Formula: C₇H₇BrClN

Purity: 95%

Color and Shape: Solid

Molecular weight: 220.49

Ref: 10-F024553

4-Bromo-3-chloro-2-methylaniline

CAS: 627531-47-9

4-Bromo-3-chloro-2-methylaniline is a heterocyclic compound that is used in organic synthesis. It is a precursor in the preparation of saccharin, indoxyls and other heterocycles, as well as glycosylations. 4-Bromo-3-chloro-2-methylaniline can be prepared by the transfer of chlorine from chlorosulfonic acid to an alkene with bromine. The reaction yields a mixture of products, including glycosylations. This process can be monitored using thin layer chromatography or by enzymatic hydrolysis. The yield of this reaction is low, so it may need to be scaled up for industrial applications. 4-Bromo-3-chloro-2-methylaniline can also be prepared from indoxyls using halides. This process is mediated by sodium methoxide and potassium tetrach

Formula: C₇H₇BrClN

Purity: Min. 95%

Molecular weight: 220.49 g/mol

Ref: 3D-CAB53147