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Catalog Number:
02869
CAS Number:
142335-42-0
Ácido Boc-(3 S -1,2,3,4-tetrahidroisoquinolin-7-hidroxi-3-carboxílico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-Tic(OH)-OH, Boc-7-hidroxi-L-Tic-OH, Boc-Tic(OH)-OH
Documents
$85.00 /250 mg
Tamaño
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Product Information

Boc-(3S)-1,2,3,4-tetrahydroisoquinoline-7-hydroxy-3-carboxylic acid is a versatile compound widely utilized in pharmaceutical research and organic synthesis. This compound features a unique structure that includes a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal candidate for various chemical transformations. Its hydroxyl and carboxylic acid functional groups contribute to its potential as a building block in the synthesis of bioactive molecules, particularly in the development of novel therapeutic agents targeting neurological disorders.

Researchers appreciate this compound for its ability to facilitate complex reactions while maintaining high selectivity and yield. Its applications extend to the synthesis of isoquinoline derivatives, which are known for their diverse biological activities, including anti-inflammatory and analgesic properties. The compound's favorable properties make it an essential tool for medicinal chemists and researchers aiming to explore new pharmacological avenues.

Synonyms
Boc-L-Tic(OH)-OH, Boc-7-hidroxi-L-Tic-OH, Boc-Tic(OH)-OH
CAS Number
142335-42-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 15 H 19 N.º 5
Molecular Weight
293.3
MDL Number
MFCD00671683
PubChem ID
381020
Melting Point
188-194 ºC
Appearance
Polvo blanco
Optical Rotation
=+ 16 ± 2 º (C=0,7 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-Tic(OH)-OH, Boc-7-hidroxi-L-Tic-OH, Boc-Tic(OH)-OH
CAS Number
142335-42-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 15 H 19 N.º 5
Molecular Weight
293.3
MDL Number
MFCD00671683
PubChem ID
381020
Melting Point
188-194 ºC
Appearance
Polvo blanco
Optical Rotation
=+ 16 ± 2 º (C=0,7 en MeOH)
Conditions
Conservar entre 0 y 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-7-hydroxy-3-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Biochemical Research: It is used in studies investigating enzyme inhibition and receptor binding, providing insights into molecular interactions and potential therapeutic targets.
  • Organic Synthesis: The compound acts as a versatile building block in organic synthesis, allowing researchers to create complex molecules with improved yields and selectivity.
  • Analytical Chemistry: It is employed in the development of analytical methods for detecting and quantifying isoquinoline derivatives, aiding in quality control and research validation.
  • Material Science: The compound is explored for its potential applications in creating novel materials with unique properties, contributing to advancements in nanotechnology and polymer science.

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