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Catalog Number:
05011
CAS Number:
178432-50-3
Ácido Fmoc-(3 R -1,2,3,4-tetrahidroisoquinolin-7-hidroxi-3-carboxílico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-Tic(OH)-OH, Fmoc-7-hidroxi-D-Tic-OH
Documents
$65.40 /100 mg
Tamaño
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Product Information

Fmoc-(3R)-1,2,3,4-tetrahydroisoquinoline-7-hydroxy-3-carboxylic acid is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound, often referred to as Fmoc-THIQ, serves as a valuable building block in the development of peptide-based therapeutics and other bioactive molecules. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, facilitates the selective modification of amino acids, making it an essential tool for researchers engaged in peptide synthesis.

The compound's hydroxyl and carboxylic acid functional groups enhance its reactivity, allowing for diverse applications in drug discovery and development. Researchers have successfully employed Fmoc-THIQ in the synthesis of complex natural products and in the design of novel therapeutic agents targeting various diseases. Its ability to provide stability and solubility in biological systems further underscores its importance in pharmaceutical formulations. With its unique properties and practical applications, Fmoc-(3R)-1,2,3,4-tetrahydroisoquinoline-7-hydroxy-3-carboxylic acid stands out as a crucial compound for advancing research and innovation in the chemical and pharmaceutical industries.

Synonyms
Fmoc-D-Tic(OH)-OH, Fmoc-7-hidroxi-D-Tic-OH
CAS Number
178432-50-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C 25 H 21 N.º 5
Molecular Weight
415.4
MDL Number
MFCD00792390
PubChem ID
4687522
Melting Point
192-198? C
Optical Rotation
-29 ± 1º (c=0,55% en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-Tic(OH)-OH, Fmoc-7-hidroxi-D-Tic-OH
CAS Number
178432-50-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C 25 H 21 N.º 5
Molecular Weight
415.4
MDL Number
MFCD00792390
PubChem ID
4687522
Melting Point
192-198? C
Optical Rotation
-29 ± 1º (c=0,55% 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

Fmoc-(3R)-1,2,3,4-tetrahydroisoquinoline-7-hydroxy-3-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without affecting other functional groups.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Biochemical Research: Researchers use this chemical to study enzyme interactions and metabolic pathways, providing insights into cellular functions and disease mechanisms.
  • Material Science: It is applied in the development of advanced materials, such as polymers and nanomaterials, which can be tailored for specific applications in electronics and coatings.
  • Natural Product Synthesis: The compound is involved in synthesizing complex natural products, facilitating the exploration of bioactive compounds with potential medicinal properties.

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