CAS 102185-48-8

5-bromo-6-chloro-3-indolyl acetate

Description:

5-Bromo-6-chloro-3-indolyl acetate is a synthetic organic compound that belongs to the class of indole derivatives. It is characterized by the presence of both bromine and chlorine substituents on the indole ring, which contribute to its unique chemical properties and reactivity. The acetate group enhances its solubility in organic solvents and can influence its biological activity. This compound is often utilized in biochemical research, particularly in studies involving enzyme activity and as a substrate in various assays due to its ability to undergo hydrolysis. Its structural features allow it to participate in electrophilic aromatic substitution reactions, making it a valuable intermediate in organic synthesis. Additionally, the presence of halogen atoms can impart specific electronic effects, potentially affecting the compound's interaction with biological targets. Safety data should be consulted before handling, as halogenated compounds can pose health risks. Overall, 5-bromo-6-chloro-3-indolyl acetate is an important compound in the field of medicinal chemistry and biochemistry.

Formula: C₁₀H₇BrClNO₂

1H-Indol-3-ol, 5-bromo-6-chloro-, 3-acetate

CAS: 102185-48-8

Formula: C₁₀H₇BrClNO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 288.5251

Ref: IN-DA0006U2

5-Bromo-6-chloro-3-indoxyl-3-acetate

CAS: 102185-48-8

5-Bromo-6-chloro-3-indoxyl-3-acetate

Purity: 98%

Color and Shape: Solid

Molecular weight: 288.53g/mol

Ref: 54-BIB1472

5-Bromo-6-chloro-3-indolyl acetate

CAS: 102185-48-8

5-Bromo-6-chloro-3-indolyl acetate is a chromogenic substrate that yields a magenta-colored product after cleavage. The chromophore 5-bromo-6-chloro-indoxyl is released, generating the observable color. It is used in bacterial esterase detection (e.g. Staphylococcus spp.).

Formula: C₁₀H₇BrClNO₂

Purity: Min. 98 Area-%

Color and Shape: Powder

Molecular weight: 288.52 g/mol

Ref: 3D-EB30201

5-Bromo-6-chloro-3-indoxyl-3-acetate

CAS: 102185-48-8

Chromogenic substrate for carboxylesterase yielding a magenta precipitate upon cleavage. Mainly used in histochemistry.

Formula: C₁₀H₇BrClNO₂

Purity: Min. 98.0 Area-%

Molecular weight: 288.53 g/mol

Ref: 3D-B-6304

5-Bromo-6-chloro-1H-indol-3-yl acetate

CAS: 102185-48-8

Formula: C₁₀H₇BrClNO₂

Purity: 98%

Molecular weight: 288.53

Ref: 10-F224526