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Catalog Number:
15348
CAS Number:
270062-99-2
Fmoc-(S-2-tetrahydroisoquinoline acetic acid
Purity:
≥ 99%
Synonym(s):
Fmoc-Tqa-OH, Fmoc-(S-1,2,3,4-tetrahydroisoquinoline-3-acetic acid
Documents
$100.05 /100MG
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Product Information

Fmoc-(S)-2-tetrahydroisoquinoline acetic acid is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound features a unique Fmoc (fluorenylmethyloxycarbonyl) protecting group, which is essential for the selective protection of amines during peptide synthesis. Its structure allows for efficient incorporation into various peptide sequences, making it an invaluable tool for researchers focused on developing novel therapeutic agents. The compound's ability to facilitate the formation of complex structures enhances its relevance in drug discovery and development, particularly in the synthesis of bioactive peptides and small molecules.

In addition to its applications in peptide synthesis, Fmoc-(S)-2-tetrahydroisoquinoline acetic acid has shown potential in the development of targeted therapies due to its structural properties. Researchers can leverage its unique characteristics to explore new avenues in medicinal chemistry, particularly in the design of isoquinoline-based compounds that exhibit promising biological activities. This compound stands out for its stability and ease of use, making it a preferred choice for professionals in pharmaceutical research and development.

Synonyms
Fmoc-Tqa-OH, Fmoc-(S-1,2,3,4-tetrahydroisoquinoline-3-acetic acid
CAS Number
270062-99-2
Purity
≥ 99%
Molecular Formula
C26H23NO4
Molecular Weight
413.47
MDL Number
MFCD01861032
PubChem ID
53397993
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-Tqa-OH, Fmoc-(S-1,2,3,4-tetrahydroisoquinoline-3-acetic acid
CAS Number
270062-99-2
Purity
≥ 99%
Molecular Formula
C26H23NO4
Molecular Weight
413.47
MDL Number
MFCD01861032
PubChem ID
53397993
Appearance
White powder
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

Fmoc-(S)-2-tetrahydroisoquinoline acetic 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 makes it valuable in the design of novel pharmaceuticals, particularly in developing compounds that target specific biological pathways.
  • Bioconjugation: The chemical is employed in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Research in Neuroscience: It plays a role in the synthesis of compounds that may influence neurological pathways, aiding in the development of treatments for neurodegenerative diseases.
  • Analytical Chemistry: The compound is used in analytical methods for detecting and quantifying specific biomolecules, improving the accuracy of biochemical assays.

Citations