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Catalog Number:
02599
CAS Number:
78879-20-6
Boc-(3S-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-L-Tic-OH, Boc-Tic-OH
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Product Information

Boc-(3S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid is a versatile compound widely utilized in pharmaceutical research and organic synthesis. This compound serves as a crucial building block in the development of various bioactive molecules, particularly in the synthesis of isoquinoline derivatives, which are known for their diverse pharmacological activities. Its unique structure, featuring a Boc (tert-butyloxycarbonyl) protecting group, enhances its stability and reactivity, making it an ideal candidate for peptide synthesis and medicinal chemistry applications. Researchers appreciate its role in facilitating the creation of complex molecules, thereby accelerating drug discovery processes.

In addition to its utility in synthetic chemistry, Boc-(3S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid is also recognized for its potential in developing novel therapeutic agents. Its ability to act as a chiral building block allows for the synthesis of enantiomerically pure compounds, which is essential in the pharmaceutical industry for ensuring efficacy and safety in drug formulations. The compound's favorable properties and applications make it a valuable asset for researchers and industry professionals looking to innovate in drug development and synthesis.

Synonyms
Boc-L-Tic-OH, Boc-Tic-OH
CAS Number
78879-20-6
Purity
≥ 98% (HPLC)
Molecular Formula
C15H19NO4
Molecular Weight
277.3
MDL Number
MFCD00143845
PubChem ID
6921826
Melting Point
125 - 130 °C
Appearance
White powder
Optical Rotation
[a]20D = 18 ± 2 ° (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-Tic-OH, Boc-Tic-OH
CAS Number
78879-20-6
Purity
≥ 98% (HPLC)
Molecular Formula
C15H19NO4
Molecular Weight
277.3
MDL Number
MFCD00143845
PubChem ID
6921826
Melting Point
125 - 130 °C
Appearance
White powder
Optical Rotation
[a]20D = 18 ± 2 ° (C=1 in MeOH)
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

Boc-(3S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders. Its unique structure allows for the development of drugs with improved efficacy.
  • Peptide Chemistry: It is commonly used in peptide synthesis as a protecting group for amino acids, facilitating the formation of complex peptide chains while preventing unwanted reactions.
  • Research in Neuroscience: The compound is valuable in neuroscience research for studying neurotransmitter systems and developing potential treatments for conditions like depression and anxiety.
  • Organic Synthesis: Its application in organic synthesis enables chemists to create diverse chemical libraries, which are essential for drug discovery and development processes.
  • Biochemical Studies: The compound is utilized in biochemical assays to investigate enzyme activity and interactions, contributing to a better understanding of metabolic pathways.

Citations