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Catalog Number:
06890
CAS Number:
79815-20-6
L-Indoline-2-carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
(S)-(-)-Indoline-2-carboxylic acid, (S)-2,3-Dihydro-1H-indole-2-carboxylic acid
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Product Information

L-Indoline-2-carboxylic acid is a versatile compound recognized for its significant role in organic synthesis and pharmaceutical applications. This compound, characterized by its indole structure, is particularly valuable in the development of various bioactive molecules. Its unique properties make it an essential building block in the synthesis of indole derivatives, which are widely used in the production of pharmaceuticals, agrochemicals, and dyes. Researchers appreciate L-Indoline-2-carboxylic acid for its ability to facilitate complex reactions, leading to the creation of compounds with enhanced biological activity.

In the pharmaceutical industry, L-Indoline-2-carboxylic acid has been utilized in the synthesis of potential therapeutic agents, including anti-inflammatory and anti-cancer drugs. Its application extends to the development of novel materials in organic electronics and photonic devices, showcasing its versatility beyond traditional uses. The compound's stability and reactivity make it an attractive choice for researchers looking to innovate in drug discovery and materials science. With its broad range of applications, L-Indoline-2-carboxylic acid stands out as a crucial component for professionals aiming to advance their projects in medicinal chemistry and related fields.

Synonyms
(S)-(-)-Indoline-2-carboxylic acid, (S)-2,3-Dihydro-1H-indole-2-carboxylic acid
CAS Number
79815-20-6
Purity
≥ 98% (HPLC)
Molecular Formula
C9H9NO2
Molecular Weight
163.18
MDL Number
MFCD00070578
PubChem ID
86074
Melting Point
163 - 170 °C
Appearance
Off-white to yellowish crystalline powder
Optical Rotation
[a]D20 = -115 ± 3º
Conditions
Store at 0 - 8 °C
General Information
Synonyms
(S)-(-)-Indoline-2-carboxylic acid, (S)-2,3-Dihydro-1H-indole-2-carboxylic acid
CAS Number
79815-20-6
Purity
≥ 98% (HPLC)
Molecular Formula
C9H9NO2
Molecular Weight
163.18
MDL Number
MFCD00070578
PubChem ID
86074
Melting Point
163 - 170 °C
Appearance
Off-white to yellowish crystalline powder
Optical Rotation
[a]D20 = -115 ± 3º
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

L-Indoline-2-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Organic Synthesis: It is employed in organic chemistry for creating complex molecules, allowing researchers to explore new chemical reactions and pathways.
  • Material Science: The compound is used in the production of advanced materials, including polymers and coatings, enhancing their properties such as durability and resistance.
  • Biochemical Research: It plays a role in studying enzyme mechanisms and metabolic pathways, providing insights into biological processes and potential therapeutic targets.
  • Analytical Chemistry: L-Indoline-2-carboxylic acid is utilized as a standard in analytical methods, aiding in the accurate quantification of related compounds in various samples.

Citations