Dibenzyl 2-[[4-oxo-4-phenylmethoxy-2-(phenylmethoxycarbonylamino)butanoyl]amino]butanedioate

Base Information

Chemical Name:Dibenzyl 2-[[4-oxo-4-phenylmethoxy-2-(phenylmethoxycarbonylamino)butanoyl]amino]butanedioate
CAS No.:4526-73-2
Molecular Formula:C₃₇H₃₆N₂O₉
Molecular Weight:652.701
Hs Code.:
NSC Number:120021
DSSTox Substance ID:DTXSID60297999

Synonyms:4526-73-2;NSC120021;DTXSID60297999;NSC-120021;dibenzyl 2-[[4-oxo-4-phenylmethoxy-2-(phenylmethoxycarbonylamino)butanoyl]amino]butanedioate

Suppliers and Price of Dibenzyl 2-[[4-oxo-4-phenylmethoxy-2-(phenylmethoxycarbonylamino)butanoyl]amino]butanedioate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of Dibenzyl 2-[[4-oxo-4-phenylmethoxy-2-(phenylmethoxycarbonylamino)butanoyl]amino]butanedioate

Chemical Property:

Vapor Pressure:1.3E-27mmHg at 25°C
Boiling Point:828.7°C at 760 mmHg
Flash Point:455°C
Density:1.266g/cm³
XLogP3:4.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:20
Exact Mass:652.24208073
Heavy Atom Count:48
Complexity:1010

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC(=O)CC(C(=O)NC(CC(=O)OCC2=CC=CC=C2)C(=O)OCC3=CC=CC=C3)NC(=O)OCC4=CC=CC=C4

Technology Process of Dibenzyl 2-[[4-oxo-4-phenylmethoxy-2-(phenylmethoxycarbonylamino)butanoyl]amino]butanedioate

There total 2 articles about Dibenzyl 2-[[4-oxo-4-phenylmethoxy-2-(phenylmethoxycarbonylamino)butanoyl]amino]butanedioate 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:

: 3479-47-8
Z-Asp(OBzl)-OH

: 4526-73-2
N-(O-benzyl-N-benzyloxycarbonyl-L-α-aspartyl)-L-aspartic acid dibenzyl ester

Guidance literature:: With dichloromethane; triethylamine; dicyclohexyl-carbodiimide;

Reference yield:

: 5241-60-1
di(phenylmethyl) (2S)-2-[(phenylmethoxy)carbonylamino]-butane-1,4-dioate

: 4526-73-2
N-(O-benzyl-N-benzyloxycarbonyl-L-α-aspartyl)-L-aspartic acid dibenzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous acetone; LiOH

2: triethylamine; dicyclohexylcarbodiimide; CH₂Cl₂

With lithium hydroxide; dichloromethane; triethylamine; dicyclohexyl-carbodiimide; acetone;