6-Chloro-3-indolyl acetate is a chemical compound that belongs to the class of indole derivatives, which are known for their diverse biological activities. This compound features a chloro substituent at the 6-position of the indole ring and an acetate group, contributing to its reactivity and potential applications in various fields, including biochemistry and medicinal chemistry. It is often utilized as a substrate in enzymatic assays, particularly for the detection of certain enzymes like β-glucuronidase, due to its ability to release a colored product upon hydrolysis. The presence of the chloro group can influence the compound's solubility and reactivity, making it a valuable tool in synthetic organic chemistry. Additionally, its structural characteristics may impart specific interactions with biological targets, making it of interest in pharmacological research. As with many chemical substances, proper handling and safety precautions are essential, given its potential biological activity and the need for thorough understanding of its properties in experimental contexts.

6-CHLORO-3-INDOLYL ACETATE

114305-99-6: 6-Chloro-3-indolyl acetate is a chemical compound that belongs to the class of indole derivatives, which are known for their diverse biological activities. This compound features a chloro substituent at the 6-position of the indole ring and an acetate group, contributing to its reactivity and potential applications in various fields, including biochemistry and medicinal chemistry. It is often utilized as a substrate in enzymatic assays, particularly for the detection of certain enzymes like β-glucuronidase, due to its ability to release a colored product upon hydrolysis. The presence of the chloro group can influence the compound's solubility and reactivity, making it a valuable tool in synthetic organic chemistry. Additionally, its structural characteristics may impart specific interactions with biological targets, making it of interest in pharmacological research. As with many chemical substances, proper handling and safety precautions are essential, given its potential biological activity and the need for thorough understanding of its properties in experimental contexts.

6-Chloro-1H-indol-3-yl acetate

6-Chloro-3-indolyl acetate

<p>Chromogenic substrate for carboxylesterase yielding a salmon colored precipitate upon cleavage. Mainly used in histochemistry.</p>

6-Chloro-3-indoxyl-3-acetate

<p>6-Chloro-3-indoxyl-3-acetate is a chromogenic substrate for carboxylesterase yielding a salmon colored precipitate upon cleavage. Mainly used in histochemistry.</p>

CAS 114305-99-6

6-CHLORO-3-INDOLYL ACETATE

6-Chloro-1H-indol-3-yl acetate

Ref: IN-DA000B1J

6-Chloro-3-indolyl acetate

Ref: 54-BIC1358

6-Chloro-3-indoxyl-3-acetate

Ref: 3D-C-4758

6-Chloro-3-indoxyl-3-acetate

Ref: 3D-EC32010