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Catalog Number:
41461
CAS Number:
141410-06-2
(S)-(+)-Methyl indoline-2-carboxylate
Purity:
≥ 97% (HPLC)
Synonym(s):
(S)-2,3-Dihydro-1H-indole-2-carboxylic acid methyl ester, (S)-Indoline-2-carboxylic acid methyl ester
Hazmat
Documents
$130.60 /500MG
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Product Information

(S)-(+)-Methyl indoline-2-carboxylate is a versatile compound recognized for its significant applications in pharmaceutical research and organic synthesis. This chiral molecule serves as an important building block in the development of various bioactive compounds, particularly in the synthesis of indole derivatives, which are known for their diverse biological activities, including anti-inflammatory and anticancer properties. Its unique stereochemistry enhances its utility in asymmetric synthesis, making it a valuable asset for researchers aiming to create enantiomerically pure compounds.

In addition to its role in drug discovery, (S)-(+)-Methyl indoline-2-carboxylate is also utilized in the production of agrochemicals and fine chemicals, where its ability to participate in various chemical reactions can lead to the formation of complex molecular architectures. The compound's favorable reactivity and stability under standard laboratory conditions make it an ideal choice for both academic and industrial applications. Researchers and industry professionals can leverage this compound to streamline their synthesis processes and enhance the efficacy of their products.

Synonyms
(S)-2,3-Dihydro-1H-indole-2-carboxylic acid methyl ester, (S)-Indoline-2-carboxylic acid methyl ester
CAS Number
141410-06-2
Purity
≥ 97% (HPLC)
Molecular Formula
C10H11NO2
Molecular Weight
0
MDL Number
MFCD12796094
PubChem ID
2794655
Appearance
Crystals
Optical Rotation
[á]/D = 31.0 ± 1.5 ° (C = 1 in Chloroform)
Conditions
Store at RT
General Information
Synonyms
(S)-2,3-Dihydro-1H-indole-2-carboxylic acid methyl ester, (S)-Indoline-2-carboxylic acid methyl ester
CAS Number
141410-06-2
Purity
≥ 97% (HPLC)
Molecular Formula
C10H11NO2
Molecular Weight
0
MDL Number
MFCD12796094
PubChem ID
2794655
Appearance
Crystals
Optical Rotation
[á]/D = 31.0 ± 1.5 ° (C = 1 in Chloroform)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-(+)-Methyl indoline-2-carboxylate is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly in the development of drugs targeting neurological disorders.
  • Organic Synthesis: It is employed in organic synthesis as a building block for creating complex molecules, allowing chemists to design and produce new compounds with desired properties.
  • Material Science: The compound is used in the formulation of advanced materials, such as polymers and coatings, enhancing their mechanical and thermal properties.
  • Agricultural Chemistry: It finds applications in the development of agrochemicals, contributing to the design of more effective pesticides and herbicides that are environmentally friendly.
  • Biochemical Research: Researchers utilize this compound in biochemical studies to explore its interactions with biological systems, aiding in the understanding of metabolic pathways.

Citations