CAS 160233-76-1

6-bromoquinoline-4-carboxylic acid

Description:

6-Bromoquinoline-4-carboxylic acid is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a bromine atom at the 6-position and a carboxylic acid group at the 4-position contributes to its unique chemical properties. This compound typically exhibits moderate solubility in polar solvents due to the carboxylic acid functionality, while its aromatic nature allows for potential π-π interactions. It may participate in various chemical reactions, including electrophilic substitutions and coupling reactions, making it valuable in synthetic organic chemistry. Additionally, the bromine substituent can serve as a useful handle for further functionalization. 6-Bromoquinoline-4-carboxylic acid may also exhibit biological activity, as many quinoline derivatives are known for their pharmacological properties, including antimicrobial and antitumor activities. Its specific applications can vary, but it is often utilized in the development of pharmaceuticals, agrochemicals, and as a building block in organic synthesis.

Formula: C₁₀H₆BrNO₂

InChI: InChI=1/C10H6BrNO2/c11-6-1-2-9-8(5-6)7(10(13)14)3-4-12-9/h1-5H,(H,13,14)

SMILES: c1cc2c(cc1Br)c(ccn2)C(=O)O

Synonyms:

• 4-Quinolinecarboxylic Acid, 6-Bromo-

4-Quinolinecarboxylic acid, 6-bromo-

CAS: 160233-76-1

Formula: C₁₀H₆BrNO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 252.0641

Ref: IN-DA001RSH

6-Bromo-4-quinolinecarboxylic acid

CAS: 160233-76-1

6-Bromo-4-quinolinecarboxylic acid

Purity: 98%

Molecular weight: 252.067g/mol

Ref: 54-OR74534

6-Bromoquinoline-4-carboxylic acid

CAS: 160233-76-1

Formula: C₁₀H₆BrNO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 252.067

Ref: 10-F214731