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Catalog Number:
19102
CAS Number:
172595-67-4
5-Chloro-1H-indole-3-carboxylic acid methyl ester
Purity:
≥ 98% (Assay)
Synonym(s):
Methyl 5-chloro-1H-indole-3-carboxylate
Documents
$89.13 /100MG
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Product Information

5-Chloro-1H-indole-3-carboxylic acid methyl ester is a versatile compound widely utilized in pharmaceutical and chemical research. This methyl ester derivative of 5-chloro-1H-indole-3-carboxylic acid is known for its unique structural properties, which make it an essential building block in the synthesis of various bioactive molecules. Its ability to act as an intermediate in the production of indole-based pharmaceuticals highlights its significance in drug development, particularly in the creation of compounds with potential anti-inflammatory and anticancer properties.

In addition to its pharmaceutical applications, this compound is also valuable in the field of organic synthesis, where it serves as a key reagent in the preparation of more complex chemical structures. Researchers appreciate its stability and reactivity, which facilitate efficient synthetic pathways. The compound's favorable characteristics, such as its solubility and compatibility with various reaction conditions, make it an attractive choice for both academic and industrial applications.

Synonyms
Methyl 5-chloro-1H-indole-3-carboxylate
CAS Number
172595-67-4
Purity
≥ 98% (Assay)
Molecular Formula
C10H8ClNO2
Molecular Weight
209.63
MDL Number
MFCD06203871
PubChem ID
15859771
Appearance
Off-white to pinkish solid
Conditions
Store at 0-8 °C
General Information
Synonyms
Methyl 5-chloro-1H-indole-3-carboxylate
CAS Number
172595-67-4
Purity
≥ 98% (Assay)
Molecular Formula
C10H8ClNO2
Molecular Weight
209.63
MDL Number
MFCD06203871
PubChem ID
15859771
Appearance
Off-white to pinkish solid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Chloro-1H-indole-3-carboxylic acid methyl ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing drugs targeting neurological disorders.
  • Biochemical Research: It is used in studies investigating the mechanisms of action of indole derivatives, contributing to advancements in understanding cellular processes.
  • Agricultural Chemistry: The compound has potential applications in creating agrochemicals, enhancing crop protection products through its biological activity against pests.
  • Material Science: It can be incorporated into polymer formulations, improving the properties of materials used in coatings and adhesives.
  • Analytical Chemistry: This chemical is employed as a standard in analytical methods, aiding in the detection and quantification of similar indole derivatives in complex mixtures.

Citations