14010

O-Benzyl-L-tyrosine

≥99.0% (NT), for peptide synthesis

• Synonyme(s) : 4-Benzyloxy-L-phenylalanine
• Formule linéaire : C₆H₅CH₂OC₆H₄CH₂CH(NH₂)CO₂H
• Numéro CAS: 16652-64-5
• Poids moléculaire : 271.31
• Numéro Beilstein : 2659642
• Numéro CE : 240-699-1
• Numéro MDL: MFCD00002605
• Code UNSPSC : 12352200
• ID de substance PubChem : 329750389
• Nomenclature NACRES : NA.22

Propriétés

• product name: O-Benzyl-L-tyrosine, ≥99.0% (NT)
• Pureté: ≥99.0% (NT)
• Activité optique: [α]20/D −9.5±1°, c = 1% in acetic acid: water (4:1)
• Capacité de réaction: reaction type: solution phase peptide synthesis
• Pf: 259 °C (dec.) (lit.)
• Application(s): peptide synthesis
• Groupe fonctionnel: amine; carboxylic acid; phenyl
• Chaîne SMILES: N[C@@H](Cc1ccc(OCc2ccccc2)cc1)C(O)=O
• InChI: 1S/C16H17NO3/c17-15(16(18)19)10-12-6-8-14(9-7-12)20-11-13-4-2-1-3-5-13/h1-9,15H,10-11,17H2,(H,18,19)/t15-/m0/s1
• Clé InChI: KAFHLONDOVSENM-HNNXBMFYSA-N
• Informations sur le gène: human ... PPARG(5468)

Description

Description générale

O-Benzyl-L-tyrosine is a derivative of the natural amino acid tyrosine. It is used as a building block in a variety of applications, including solution-phase peptide synthesis, and the production of pharmaceuticals and other chemicals.

Application

O-Benzyl-L-tyrosine can be used as a building block in the synthesis of amphiphilic block co-polypeptides, due to their potential applications in biomedical fields. For instance, it is used to prepare Lysine-block-tyrosine block copolypeptides, which are useful as targeted drug carriers, functional nanobioreactors, and biomimetic encapsulants in the biomedical fields.

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable
• Équipement de protection individuelle: Eyeshields, Gloves, type N95 (US)