CAS 1356483-77-6: 4-Bromo-N2-cyclopropyl-1,2-benzenediamine

Description: 4-Bromo-N2-cyclopropyl-1,2-benzenediamine is an organic compound characterized by its unique structure, which includes a bromine atom and a cyclopropyl group attached to a benzene ring with two amine functional groups. The presence of the bromine substituent enhances its reactivity and may influence its biological activity, making it of interest in medicinal chemistry. The cyclopropyl group contributes to the compound's three-dimensional shape, potentially affecting its interaction with biological targets. This compound is likely to exhibit properties typical of amines, such as basicity and the ability to form hydrogen bonds, which can influence its solubility and reactivity in various chemical environments. Additionally, the presence of multiple functional groups suggests that it may participate in a range of chemical reactions, including nucleophilic substitutions and coupling reactions. Its specific applications and behavior would depend on the context of its use, particularly in pharmaceutical research or synthetic organic chemistry. Safety and handling considerations should be taken into account due to the presence of bromine and the potential for biological activity.

Formula: C₉H₁₁BrN₂

InChI: InChI=1S/C9H11BrN2/c10-6-1-4-8(11)9(5-6)12-7-2-3-7/h1,4-5,7,12H,2-3,11H2

InChI key: InChIKey=OWPZYOFPXATQIS-UHFFFAOYSA-N

SMILES: BrC1=CC=C(N)C(=C1)NC2CC2

Synonyms:

• 4-Bromo-N2-cyclopropyl-1,2-benzenediamine
• 5-Bromo-N-cyclopropylbenzene-1,2-diamine
• 1,2-Benzenediamine, 4-bromo-N2-cyclopropyl-

5-Bromo-N1-cyclopropylbenzene-1,2-diamine

CAS: 1356483-77-6

• Purity: 95%
• Molecular weight: 227.10499572753906

5-Bromo-N1-cyclopropylbenzene-1,2-diamine

CAS: 1356483-77-6

Versatile small molecule scaffold

• Formula: C₉H₁₁BrN₂
• Purity: Min. 95%
• Molecular weight: 227.1 g/mol