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Catalog Number:
19432
CAS Number:
79799-05-6
S-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid methyl ester
Synonym(s):
(S-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid methyl ester, Methyl 1,2,3,4-tetrahydroisoquinoline-3(S)-carboxylate
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Product Information

(S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid methyl ester is a versatile compound with significant relevance in pharmaceutical research and development. This chiral molecule is recognized for its potential as a building block in the synthesis of various bioactive compounds, particularly in the field of medicinal chemistry. Its unique structure allows for the exploration of new therapeutic agents, particularly those targeting neurological disorders and pain management. Researchers appreciate its ability to serve as a precursor in the synthesis of isoquinoline derivatives, which are known for their diverse biological activities, including anti-inflammatory and analgesic properties.

In addition to its applications in drug development, (S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid methyl ester is also utilized in the study of receptor interactions and enzyme inhibition, making it a valuable tool for scientists investigating complex biochemical pathways. Its favorable solubility and stability further enhance its utility in laboratory settings, allowing for efficient handling and experimentation. This compound stands out in its category due to its chiral nature, which can lead to the development of more selective and effective therapeutic agents compared to non-chiral counterparts.

Synonyms
(S-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid methyl ester, Methyl 1,2,3,4-tetrahydroisoquinoline-3(S)-carboxylate
CAS Number
79799-05-6
Molecular Formula
C11H13NO2
Molecular Weight
191.23
MDL Number
MFCD03419266
PubChem ID
4685119
Conditions
Store at 0-8°C
General Information
Synonyms
(S-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid methyl ester, Methyl 1,2,3,4-tetrahydroisoquinoline-3(S)-carboxylate
CAS Number
79799-05-6
Molecular Formula
C11H13NO2
Molecular Weight
191.23
MDL Number
MFCD03419266
PubChem ID
4685119
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

(S)-1,2,3,4-Tetrahydroisoquinoline-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 the development of drugs targeting neurological disorders.
  • Organic Synthesis: It is used in organic chemistry for constructing complex molecules, offering a versatile building block for researchers looking to create novel compounds.
  • Biochemical Research: The compound is employed in studies exploring enzyme interactions and metabolic pathways, helping scientists understand biological processes at a molecular level.
  • Material Science: It finds applications in developing new materials, especially in creating polymers with specific properties, enhancing performance in various industrial applications.
  • Natural Product Synthesis: Researchers utilize this compound in the synthesis of natural products, which can lead to the discovery of new bioactive compounds with potential therapeutic effects.

Citations