CAS 32435-61-3

4-Bromo-3-quinolinol

Description:

4-Bromo-3-quinolinol, with the CAS number 32435-61-3, is a chemical compound that belongs to the class of quinolinols, which are derivatives of quinoline featuring a hydroxyl group. This compound is characterized by the presence of a bromine atom at the 4-position and a hydroxyl group at the 3-position of the quinoline ring. It typically appears as a solid or crystalline substance and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. The compound may exhibit properties such as antimicrobial, antiviral, or anticancer activities, although specific biological effects can vary based on structural modifications and the presence of other functional groups. Additionally, 4-Bromo-3-quinolinol may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in organic synthesis. As with many chemical substances, handling should be done with care, considering safety data and potential hazards associated with brominated compounds.

Formula: C₉H₆BrNO

InChI: InChI=1S/C9H6BrNO/c10-9-6-3-1-2-4-7(6)11-5-8(9)12/h1-5,12H

InChI key: InChIKey=BJEMWAKSVKPWBC-UHFFFAOYSA-N

SMILES: BrC=1C2=C(N=CC1O)C=CC=C2

Synonyms:

• 4-Bromo-3-hydroxyquinoline
• 3-Quinolinol, 4-bromo-
• 4-Bromo-3-quinolinol

4-Bromo-3-hydroxyquinoline

CAS: 32435-61-3

Formula: C₉H₆BrNO

Purity: 97%

Color and Shape: Solid

Molecular weight: 224.0540

Ref: IN-DA00CH92

4-Bromoquinolin-3-ol

CAS: 32435-61-3

4-Bromoquinolin-3-ol

Purity: 97%

Molecular weight: 224.05g/mol

Ref: 54-OR93587

4-Bromoquinolin-3-ol

CAS: 32435-61-3

Formula: C₉H₆BrNO

Purity: 97%

Molecular weight: 224.057

Ref: 10-F455785

4-bromoquinolin-3-ol

CAS: 32435-61-3

4-bromoquinolin-3-ol is a piperidine derivative that belongs to the group of pyrrole derivatives. It is primarily used as a reagent in organic synthesis and in the preparation of 3-bromo-5-hydroxypyridine, 2-amino-4-hydroxypyridine, and 3-amino-2-bromopyridine. 4BQ3H is an isomeric nucleus with substitutions on the 2-, 4-, or 6 positions. The hydroxy group on the 3 position can be substituted with a variety of groups such as methoxy, ethoxy, or acetoxy. The oxindole moiety can also be replaced by a piperidide moiety. Note that the aminations are reversible under basic conditions.

Formula: C₉H₆NOBr

Purity: Min. 95%

Molecular weight: 224.05 g/mol

Ref: 3D-HBA43561