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Catalog Number:
19934
CAS Number:
15861-37-7
2,3-Dihydro-1H-indole-6-carboxylic acid hydrochloride
Purity:
≥ 98% (Assay)
Synonym(s):
6-Indolinecarboxylic acid hydrochloride
Documents
$120.88 /100MG
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Product Information

2,3-Dihydro-1H-indole-6-carboxylic acid hydrochloride is a versatile compound recognized for its significant applications in pharmaceutical research and development. This hydrochloride salt form enhances the solubility and stability of the compound, making it an excellent candidate for drug formulation. Its unique structure allows it to act as a building block in the synthesis of various bioactive molecules, particularly in the development of novel therapeutic agents targeting neurological disorders and other medical conditions. Researchers have utilized this compound in studies focused on its potential neuroprotective effects, showcasing its relevance in the field of medicinal chemistry.

The compound's ability to interact with biological systems opens avenues for innovative applications in drug discovery and development. Its favorable properties, such as moderate melting point and good solubility in aqueous solutions, make it suitable for various laboratory applications. Additionally, its role as an intermediate in organic synthesis highlights its importance in creating complex chemical entities. With its promising potential, 2,3-Dihydro-1H-indole-6-carboxylic acid hydrochloride stands out as a valuable resource for researchers and industry professionals aiming to explore new therapeutic pathways.

Synonyms
6-Indolinecarboxylic acid hydrochloride
CAS Number
15861-37-7
Purity
≥ 98% (Assay)
Molecular Formula
C9H9NO2·HCl
Molecular Weight
199.63
MDL Number
MFCD09878906
PubChem ID
53407268
Appearance
White to off-white solid
Conditions
Store at 0-8 °C
General Information
Synonyms
6-Indolinecarboxylic acid hydrochloride
CAS Number
15861-37-7
Purity
≥ 98% (Assay)
Molecular Formula
C9H9NO2·HCl
Molecular Weight
199.63
MDL Number
MFCD09878906
PubChem ID
53407268
Appearance
White to off-white 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

2,3-Dihydro-1H-indole-6-carboxylic acid hydrochloride is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Biochemical Research: It is used in studies related to enzyme inhibition and receptor binding, helping researchers understand biological pathways and develop new therapeutic agents.
  • Material Science: The compound is explored for its potential in creating novel polymers and materials, offering unique properties that can improve product performance in various applications.
  • Agricultural Chemistry: It has applications in developing agrochemicals, contributing to more effective pest control solutions that are safer for the environment.
  • Analytical Chemistry: This chemical is utilized in analytical methods for detecting and quantifying other compounds, providing reliable results in quality control processes.

Citations