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Catalog Number:
37435
CAS Number:
204384-69-0
Fmoc-L-α-HomoTyr(OtBu)-OH
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-hTyr-(OtBu)-OH, Fmoc-O-tert-butyl-L-alpha-homotyrosine
Temperature Sensitive
Documents
$156.00 /100 mg
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Product Information

Fmoc-L-a-HomoTyr(OtBu)-OH is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by the presence of a tert-butyl ether group, enhances its stability and solubility, making it an ideal choice for researchers working in organic synthesis and medicinal chemistry.

In practical applications, Fmoc-L-a-HomoTyr(OtBu)-OH is particularly valuable in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its ability to facilitate the synthesis of complex peptides allows for the exploration of novel drug candidates, particularly in the fields of oncology and immunology. Researchers appreciate its compatibility with various coupling reagents and its effectiveness in solid-phase peptide synthesis, ensuring high yields and purity of the final products. This compound stands out for its ease of use and reliability, making it a preferred choice for professionals in the pharmaceutical and biotechnology industries.

Synonyms
Fmoc-hTyr-(OtBu)-OH, Fmoc-O-tert-butyl-L-alpha-homotyrosine
CAS Number
204384-69-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 29 H 315
Molecular Weight
473.57
MDL Number
MFCD01321420
PubChem ID
75627333
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -4,1 ± 2 ° (C = 1 dans DMF)
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
Fmoc-hTyr-(OtBu)-OH, Fmoc-O-tert-butyl-L-alpha-homotyrosine
CAS Number
204384-69-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 29 H 315
Molecular Weight
473.57
MDL Number
MFCD01321420
PubChem ID
75627333
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -4,1 ± 2 ° (C = 1 dans DMF)
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-L-a-HomoTyr(OtBu)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex and functional peptides.
  • Drug Development: Its unique structure aids in the development of novel pharmaceuticals, especially in the design of peptide-based drugs that target specific biological pathways.
  • Bioconjugation: The compound can be used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: Fmoc-L-a-HomoTyr(OtBu)-OH is valuable in neuroscience research for studying receptor interactions and signaling pathways due to its structural similarity to neurotransmitters.
  • Custom Synthesis Services: Many laboratories utilize this compound for custom synthesis services, providing tailored solutions for specific research needs in various fields, including biochemistry and molecular biology.

Citations