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Catalog Number:
03574
CAS Number:
214630-00-9
Acide boc-(3 R -1,2,3,4-tétrahydroisoquinoléine-7-hydroxy-3-carboxylique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-7-hydroxy-D-Tic-OH, Boc-D-Tic(OH)-OH
Documents
$86.23 /250 mg
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Product Information

Boc-(3R)-1,2,3,4-tetrahydroisoquinoline-7-hydroxy-3-carboxylic acid is a versatile compound widely utilized in pharmaceutical research and development. This compound features a unique structure that makes it an excellent candidate for the synthesis of bioactive molecules, particularly in the field of medicinal chemistry. Its ability to act as a building block in the development of isoquinoline derivatives allows researchers to explore new therapeutic avenues, especially in neuropharmacology and anti-inflammatory drug design. The Boc protecting group enhances its stability and solubility, making it easier to handle in various synthetic processes.

In addition to its synthetic applications, this compound has shown potential in the development of targeted therapies due to its structural properties. Researchers can leverage its hydroxyl and carboxylic acid functionalities to create derivatives with enhanced biological activity. The compound's unique characteristics position it as a valuable asset for professionals looking to innovate in drug discovery and development, providing a pathway to novel therapeutic agents with improved efficacy and safety profiles.

Synonyms
Boc-7-hydroxy-D-Tic-OH, Boc-D-Tic(OH)-OH
CAS Number
214630-00-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C 15 H 195
Molecular Weight
293.3
MDL Number
MFCD00792389
PubChem ID
381020
Melting Point
196-202 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[α] D 20 = -13 ± 2º (C=1 dans MeOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-7-hydroxy-D-Tic-OH, Boc-D-Tic(OH)-OH
CAS Number
214630-00-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C 15 H 195
Molecular Weight
293.3
MDL Number
MFCD00792389
PubChem ID
381020
Melting Point
196-202 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[α] D 20 = -13 ± 2º (C=1 dans MeOH)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-(3R)-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 pharmaceuticals, particularly in the development of drugs targeting neurological disorders, enhancing therapeutic efficacy.
  • Biochemical Research: It is employed in studies investigating enzyme inhibition and receptor binding, providing insights into biological pathways and potential therapeutic targets.
  • Organic Synthesis: The compound is a valuable building block in organic chemistry, facilitating the creation of complex molecular structures with diverse functionalities.
  • Material Science: It finds applications in developing innovative materials, including polymers and coatings, due to its unique chemical properties that enhance material performance.
  • Analytical Chemistry: This chemical is used in analytical methods for detecting and quantifying specific biomolecules, aiding in quality control and research applications.

Citations