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Catalog Number:
03806
CAS Number:
87694-53-9
Boc-L-phénylalanine N -méthoxy- N -méthylamide
Purity:
≥ 98 % (HPLC, pureté chirale)
Synonym(s):
Boc-L-Phe-N( OCH3 ) CH3
Documents
$51.18 /1G
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Product Information

Réduit par LiAlH4 pour donner l'aldéhyde d'acide aminé Boc correspondant.

Synonyms
Boc-L-Phe-N( OCH3 ) CH3
CAS Number
87694-53-9
Purity
≥ 98 % (HPLC, pureté chirale)
Molecular Formula
C16H24N2O4
Molecular Weight
308.4
MDL Number
MFCD00151891
PubChem ID
375614
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-L-Phe-N( OCH3 ) CH3
CAS Number
87694-53-9
Purity
≥ 98 % (HPLC, pureté chirale)
Molecular Formula
C16H24N2O4
Molecular Weight
308.4
MDL Number
MFCD00151891
PubChem ID
375614
Appearance
Solide blanc à blanc cassé
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-L-phenylalanine N-methoxy-N-methyl amide is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, which are essential in drug development and biochemistry.
  • Pharmaceutical Research: It is used in the design of new pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Biotechnology: The compound plays a role in the production of biologically active peptides, which are crucial in developing vaccines and therapeutic proteins.
  • Analytical Chemistry: It is utilized in various analytical techniques to study protein interactions and stability, providing insights into molecular behavior.
  • Cosmetic Formulations: The compound can be incorporated into cosmetic products for its potential skin benefits, contributing to the development of innovative beauty solutions.

Citations