CAS 152213-66-6

1H-Indole-3-aceticacid,6-bromo-(9CI)

Description:

1H-Indole-3-acetic acid, 6-bromo- (9CI), with the CAS number 152213-66-6, is a synthetic compound that belongs to the class of indole derivatives. It is characterized by the presence of an indole ring, which is a bicyclic structure composed of a benzene ring fused to a pyrrole ring, and an acetic acid functional group. The bromine substituent at the 6-position of the indole ring introduces halogen characteristics, which can influence the compound's reactivity and biological activity. This compound is often studied for its potential role as a plant growth regulator, as indole-3-acetic acid (IAA) is a naturally occurring auxin involved in various plant growth processes. The presence of the bromine atom may enhance or modify the biological activity compared to its non-brominated counterparts. Additionally, the compound's solubility, stability, and interaction with biological systems can be affected by its structural features, making it of interest in both agricultural and pharmaceutical research.

Formula: C₁₀H₈BrNO₂

Synonyms:

• 2-(6-bromo-1H-indol-3-yl)acetic acid
• 1H-Indole-3-acetic acid, 6-bromo-
• (6-broMo-1H-indol-3-yl)acetic acid
• 2-(6-Bromo-1H-indol-3-yl)
• 6-Bromoindole-3-acetic acid
• 6-broMo-1H-indole-3-acetic acid
• 1H-Indole-3-aceticacid,6-bromo-(9CI)

1H-Indole-3-aceticacid,6-bromo-(9CI)

CAS: 152213-66-6

Formula: C₁₀H₈BrNO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 254.0800

Ref: IN-DA007YO2

2-(6-Bromo-1H-indol-3-yl)acetic acid

CAS: 152213-66-6

2-(6-Bromo-1H-indol-3-yl)acetic acid

Purity: 97%

Molecular weight: 254.08g/mol

Ref: 54-OR94564

2-(6-Bromo-1H-indol-3-yl)acetic acid

CAS: 152213-66-6

Formula: C₁₀H₈BrNO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 254.083

Ref: 10-F091589

2-(6-Bromo-1H-indol-3-yl)acetic acid

CAS: 152213-66-6

2-(6-Bromo-1H-indol-3-yl)acetic acid (6BIAA) is a staphylococcal metabolite that has been found to be an inhibitor of the enzyme methionine sulfoxide reductase. 6BIAA is also the methyl ester of 6-bromoindole, and has been found to inhibit the growth of Staphylococcus epidermidis. 6BIAA is a natural product that can be obtained from Aplysinopsins, which are marine sponge metabolites. The structure of 6BIAA contains two aromatic rings and one carboxylic acid group. The nmr data for this compound show three singlets at δ 11.5 ppm, δ 7.4 ppm, and δ 4.2 ppm with corresponding multiplicities of 2H, 3H, and 1H respectively. These results indicate that the compound contains an aromatic ring with a hydroxyl

Purity: Min. 95%

Ref: 3D-FB41926