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Catalog Number:
21992
CAS Number:
608-08-2
Acétate d'indoxyle
Purity:
≥ 99% (RMN)
Synonym(s):
Acétate de 1 H -Indol-3-yle, 3-Acétoxyindole
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Product Information

Indoxyl acetate is a versatile chemical compound widely recognized for its applications in the fields of biochemistry and pharmaceuticals. This compound, also known as 3-acetoxyindole, serves as a valuable intermediate in the synthesis of various indole derivatives, which are crucial in the development of pharmaceuticals and agrochemicals. Its unique structure allows it to participate in a range of chemical reactions, making it an essential building block for researchers and industry professionals focused on drug discovery and development.

In addition to its synthetic utility, indoxyl acetate is utilized in biochemical assays, particularly in the study of enzyme activity and metabolic pathways. Its ability to release indoxyl upon hydrolysis makes it a useful substrate for investigating the activity of specific enzymes, such as β-glucosidases. This characteristic not only aids in research but also enhances its relevance in the agricultural sector, where it can be employed in the formulation of plant growth regulators. With its diverse applications and significant role in advancing scientific research, indoxyl acetate stands out as a compound of interest for professionals in various industries.

Synonyms
Acétate de 1 H -Indol-3-yle, 3-Acétoxyindole
CAS Number
608-08-2
Purity
≥ 99% (RMN)
Molecular Formula
C 10 H 9 NO 2
Molecular Weight
175.19
MDL Number
MFCD00014561
PubChem ID
11841
Melting Point
126 - 132 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Acétate de 1 H -Indol-3-yle, 3-Acétoxyindole
CAS Number
608-08-2
Purity
≥ 99% (RMN)
Molecular Formula
C 10 H 9 NO 2
Molecular Weight
175.19
MDL Number
MFCD00014561
PubChem ID
11841
Melting Point
126 - 132 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Indoxyl acetate is widely utilized in research focused on

  • Biochemical Research: It serves as a substrate for studying enzyme activity, particularly in the context of indole metabolism, helping researchers understand metabolic pathways.
  • Pharmaceutical Development: This compound is used in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents, providing a pathway for innovative drug formulations.
  • Analytical Chemistry: Indoxyl acetate is employed in chromatographic techniques for the separation and identification of indole derivatives, enhancing the accuracy of analytical methods in laboratories.
  • Plant Biology: It is utilized in studies examining plant growth and development, particularly in understanding the role of indole compounds in plant signaling and responses to environmental stress.
  • Colorimetric Assays: The compound is used in colorimetric assays to detect specific enzymes, offering a simple and effective method for quantifying enzyme activity in various biological samples.

Citations