CAS 1245648-36-5

7-Bromo-4-fluoro-1H-indole-2,3-dione

Description:

7-Bromo-4-fluoro-1H-indole-2,3-dione is a synthetic organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a bromine atom at the 7-position and a fluorine atom at the 4-position of the indole ring, contributing to its unique reactivity and potential biological activity. The presence of the dione functional groups (two carbonyl groups) at the 2 and 3 positions enhances its electrophilic character, making it a candidate for various chemical reactions, including nucleophilic attacks. This compound may exhibit interesting pharmacological properties, potentially acting as an intermediate in the synthesis of more complex molecules or as a lead compound in drug discovery. Its specific interactions and applications would depend on further studies, including its solubility, stability, and reactivity under different conditions. As with many halogenated compounds, it may also exhibit unique environmental and toxicological profiles that warrant careful handling and assessment.

Formula: C₈H₃BrFNO₂

InChI: InChI=1S/C8H3BrFNO2/c9-3-1-2-4(10)5-6(3)11-8(13)7(5)12/h1-2H,(H,11,12,13)

SMILES: c1cc(c2c(c1Br)NC(=O)C2=O)F

Synonyms:

• 4-Fluoro-7-bromoisatin

1H-Indole-2,3-dione, 7-bromo-4-fluoro-

CAS: 1245648-36-5

Formula: C₈H₃BrFNO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 244.0173

Ref: IN-DA000MCN

4-Fluoro-7-bromoisatin

CAS: 1245648-36-5

4-Fluoro-7-bromoisatin

Purity: 95%

Molecular weight: 244.02g/mol

Ref: 54-PC408007

7-Bromo-4-fluoroindoline-2,3-dione

CAS: 1245648-36-5

Formula: C₈H₃BrFNO₂

Purity: 97%

Molecular weight: 244.019

Ref: 10-F320258

7-Bromo-4-fluoroindoline-2,3-dione

CAS: 1245648-36-5

7-Bromo-4-fluoroindoline-2,3-dione is an experimental industrial solvent that belongs to the class of sulfates. It is a precursor for the synthesis of chloral and other potentially useful compounds. 7-Bromo-4-fluoroindoline-2,3-dione can be prepared by using a solvent system consisting of ethanol, sulfuric acid, and hydroxylamine. The intermediate 7-bromoindoline can be obtained by reacting 2 equivalents of bromine with 2 equivalents of ethyl acetate in the presence of sulfuric acid and hydroxylamine. The cyclization reaction can then be performed on 7-bromoindoline to give 7-bromo-4-fluoroindoline.

Formula: C₈H₃BrFNO₂

Purity: Min. 95%

Molecular weight: 244.02 g/mol

Ref: 3D-VZB64836