CAS RN 13033-84-6
D-phénylalanine d’ester de méthyle chlorhydrate, 98%
CAS: 13033-84-6 Formule moléculaire: C10H14ClNO2 Poids moléculaire (g/mol): 215.68 Numéro MDL: MFCD00066112 Clé InChI: SWVMLNPDTIFDDY-SBSPUUFOSA-N Synonyme: d-phenylalanine methyl ester hydrochloride,h-d-phe-ome.hcl,d-phenylalanine methyl ester hcl,h-d-phe-ome hcl,r-methyl 2-amino-3-phenylpropanoate hydrochloride,d-phenylalanine, methyl ester, hydrochloride,methyl d-phenylalaninate hydrochloride,r-phenylalanine methyl ester hydrochloride,methyl 2r-2-amino-3-phenylpropanoate hydrochloride PubChem CID: 11481330 Nom de l’IUPAC: méthyle (2R)-2-amino-3-phénylpropanoate; Chlorhydrate SOURIRES: Cl.COC(=O)[C@H](N)CC1=CC=CC=C1
D-phénylalanine d’ester de méthyle chlorhydrate, 98%
CAS: 13033-84-6 Formule moléculaire: C10H14ClNO2 Poids moléculaire (g/mol): 215.68 Numéro MDL: MFCD00066112 Clé InChI: SWVMLNPDTIFDDY-SBSPUUFOSA-N Synonyme: d-phenylalanine methyl ester hydrochloride,h-d-phe-ome.hcl,d-phenylalanine methyl ester hcl,h-d-phe-ome hcl,r-methyl 2-amino-3-phenylpropanoate hydrochloride,d-phenylalanine, methyl ester, hydrochloride,methyl d-phenylalaninate hydrochloride,r-phenylalanine methyl ester hydrochloride,methyl 2r-2-amino-3-phenylpropanoate hydrochloride PubChem CID: 11481330 Nom de l’IUPAC: méthyle (2R)-2-amino-3-phénylpropanoate; Chlorhydrate SOURIRES: Cl.COC(=O)[C@H](N)CC1=CC=CC=C1
D-Phénylalanine Ester de méthyle chlorhydrate 98,0+%, TCI America™
CAS: 13033-84-6 Formule moléculaire: C10H14ClNO2 Poids moléculaire (g/mol): 215.68 Numéro MDL: MFCD00066112 Clé InChI: SWVMLNPDTIFDDY-SBSPUUFOSA-N Synonyme: d-phenylalanine methyl ester hydrochloride,h-d-phe-ome.hcl,d-phenylalanine methyl ester hcl,h-d-phe-ome hcl,r-methyl 2-amino-3-phenylpropanoate hydrochloride,d-phenylalanine, methyl ester, hydrochloride,methyl d-phenylalaninate hydrochloride,r-phenylalanine methyl ester hydrochloride,methyl 2r-2-amino-3-phenylpropanoate hydrochloride PubChem CID: 11481330 Nom de l’IUPAC: hydrochlorure de méthyle (2R)-2-amino-3-phénylpropanoate SOURIRES: Cl.COC(=O)[C@H](N)CC1=CC=CC=C1