🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
07001
CAS Number:
204317-98-6
Fmoc-D-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-D-Tiq-OH
Documents
$100.05 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Fmoc-D-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid is a valuable compound widely utilized in the field of peptide synthesis and medicinal chemistry. This compound serves as a crucial building block for the development of bioactive peptides and pharmaceuticals, particularly in the design of peptide-based drugs. Its unique Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex peptide structures while maintaining stability during the process.

Researchers and industry professionals appreciate its versatility in various applications, including the synthesis of cyclic peptides and the development of targeted drug delivery systems. The compound's ability to enhance the solubility and bioavailability of peptides makes it an essential tool in drug formulation. Additionally, its structural features contribute to the modulation of biological activity, making it a promising candidate for further exploration in therapeutic applications. With its significant role in advancing peptide chemistry, Fmoc-D-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid stands out as a key resource for innovative research and development.

Synonyms
Fmoc-D-Tiq-OH
CAS Number
204317-98-6
Purity
≥ 98% (HPLC)
Molecular Formula
C25H21NO4
Molecular Weight
399.4
MDL Number
MFCD03788061
PubChem ID
4712565
Appearance
Amorphous white powder
Optical Rotation
[a]D = -28 ± 2º (C=1 in DMF)
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-D-Tiq-OH
CAS Number
204317-98-6
Purity
≥ 98% (HPLC)
Molecular Formula
C25H21NO4
Molecular Weight
399.4
MDL Number
MFCD03788061
PubChem ID
4712565
Appearance
Amorphous white powder
Optical Rotation
[a]D = -28 ± 2º (C=1 in DMF)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-D-1,2,3,4-tetrahydroisoquinoline-1-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 while preventing unwanted reactions.
  • Drug Development: It plays a crucial role in the design of new pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The chemical is used in bioconjugation processes, facilitating the attachment of biomolecules to drugs or imaging agents, which improves targeting and delivery in therapeutic applications.
  • Research in Neuroscience: Its derivatives are explored in studies related to neuropharmacology, helping researchers understand the mechanisms of action for various neurological disorders.
  • Material Science: The compound is investigated for developing advanced materials, such as polymers and nanomaterials, that have unique properties beneficial for electronics and coatings.

Citations