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Catalog Number:
18661
CAS Number:
1171876-52-0
Chlorhydrate d'acide 2,3-dihydro-1 H -indole-5-carboxylique
Purity:
≥ 95 % (dosage)
Synonym(s):
Chlorhydrate d'acide indoline-5-carboxylique
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$58.39 /100 mg
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Product Information

2,3-Dihydro-1H-indole-5-carboxylic acid hydrochloride is a versatile compound that has garnered attention in various fields, particularly in pharmaceutical research and organic synthesis. This hydrochloride salt form enhances the compound's solubility, making it an ideal candidate for drug formulation and biological studies. Its unique structure allows for potential applications in the development of novel therapeutic agents, especially in the treatment of neurological disorders and as a building block in the synthesis of complex organic molecules. Researchers have utilized this compound in the synthesis of indole derivatives, which are known for their diverse biological activities, including anti-inflammatory and anticancer properties.

The compound's ability to act as a precursor in the synthesis of bioactive molecules positions it as a valuable resource for medicinal chemists and researchers focused on drug discovery. Its stability and compatibility with various reaction conditions further enhance its utility in laboratory settings. With its promising applications and the potential for innovation in therapeutic development, 2,3-Dihydro-1H-indole-5-carboxylic acid hydrochloride stands out as a significant compound for professionals in the chemical and pharmaceutical industries.

Synonyms
Chlorhydrate d'acide indoline-5-carboxylique
CAS Number
1171876-52-0
Purity
≥ 95 % (dosage)
Molecular Formula
C9H9NO2 · HCl
Molecular Weight
199.63
MDL Number
MFCD09971545
PubChem ID
43810573
Appearance
Poudre marron clair
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Chlorhydrate d'acide indoline-5-carboxylique
CAS Number
1171876-52-0
Purity
≥ 95 % (dosage)
Molecular Formula
C9H9NO2 · HCl
Molecular Weight
199.63
MDL Number
MFCD09971545
PubChem ID
43810573
Appearance
Poudre marron clair
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2,3-Dihydro-1H-indole-5-carboxylic acid hydrochloride is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders. Its unique structure allows for modifications that enhance therapeutic efficacy.
  • Biochemical Research: It serves as a valuable tool in studying enzyme interactions and metabolic pathways, helping researchers understand complex biological processes and develop new treatments.
  • Material Science: The compound is explored for its potential in creating novel polymers and materials, offering advantages in durability and flexibility compared to traditional compounds.
  • Analytical Chemistry: It is used as a standard in chromatographic techniques, aiding in the accurate quantification of related compounds in various samples, which is crucial for quality control in manufacturing.
  • Natural Product Synthesis: This chemical is involved in the synthesis of natural product derivatives, providing researchers with a pathway to develop new bioactive compounds with potential therapeutic benefits.

Citations