(S)-2-Benzyloxycarbonylamino-3-(4-benzyloxy-phenyl)-propionic acid 3-oxo-2-phenyl-3H-inden-1-yl ester

Base Information

Chemical Name:(S)-2-Benzyloxycarbonylamino-3-(4-benzyloxy-phenyl)-propionic acid 3-oxo-2-phenyl-3H-inden-1-yl ester
CAS No.:75243-87-7
Molecular Formula:C₃₉H₃₁NO₆
Molecular Weight:609.678
Hs Code.:

Synonyms:(S)-2-Benzyloxycarbonylamino-3-(4-benzyloxy-phenyl)-propionic acid 3-oxo-2-phenyl-3H-inden-1-yl ester

Suppliers and Price of (S)-2-Benzyloxycarbonylamino-3-(4-benzyloxy-phenyl)-propionic acid 3-oxo-2-phenyl-3H-inden-1-yl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-2-Benzyloxycarbonylamino-3-(4-benzyloxy-phenyl)-propionic acid 3-oxo-2-phenyl-3H-inden-1-yl ester

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Technology Process of (S)-2-Benzyloxycarbonylamino-3-(4-benzyloxy-phenyl)-propionic acid 3-oxo-2-phenyl-3H-inden-1-yl ester

There total 1 articles about (S)-2-Benzyloxycarbonylamino-3-(4-benzyloxy-phenyl)-propionic acid 3-oxo-2-phenyl-3H-inden-1-yl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 62.0%

: 83-12-5
phenindione

: 86827-18-1,92455-53-3,16677-29-5
N-benzyloxycarbonyl-O-benzyl-L-tyrosine

: 75243-87-7
(S)-2-Benzyloxycarbonylamino-3-(4-benzyloxy-phenyl)-propionic acid 3-oxo-2-phenyl-3H-inden-1-yl ester

Guidance literature:: With dicyclohexyl-carbodiimide; In tetrahydrofuran; at 5 ℃; for 18h;

Reference yield:

: 75243-87-7
(S)-2-Benzyloxycarbonylamino-3-(4-benzyloxy-phenyl)-propionic acid 3-oxo-2-phenyl-3H-inden-1-yl ester

: 58822-25-6
Leu-enkephalin

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / acetic acid / tetrahydrofuran / 48 h / Ambient temperature

2: 60 percent / H₂ / 5percent Pd/C / methanol; H₂O / 24 h / 760 Torr

With hydrogen; acetic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; water;