p-nitrophenyl N-<<<6-(N-BOC-amino)hexyl>succinamido>-L-alanyl-L-alanyl-L-prolylmethyl>-N-isopropylcarbamate

Base Information

Chemical Name:p-nitrophenyl N-<<<6-(N-BOC-amino)hexyl>succinamido>-L-alanyl-L-alanyl-L-prolylmethyl>-N-isopropylcarbamate
CAS No.:157801-10-0
Molecular Formula:C₃₇H₅₇N₇O₁₁
Molecular Weight:775.9
Hs Code.:

Synonyms:p-nitrophenyl N-<<<6-(N-BOC-amino)hexyl>succinamido>-L-alanyl-L-alanyl-L-prolylmethyl>-N-isopropylcarbamate

Suppliers and Price of p-nitrophenyl N-<<<6-(N-BOC-amino)hexyl>succinamido>-L-alanyl-L-alanyl-L-prolylmethyl>-N-isopropylcarbamate

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 0 raw suppliers

Chemical Property of p-nitrophenyl N-<<<6-(N-BOC-amino)hexyl>succinamido>-L-alanyl-L-alanyl-L-prolylmethyl>-N-isopropylcarbamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of p-nitrophenyl N-<<<6-(N-BOC-amino)hexyl>succinamido>-L-alanyl-L-alanyl-L-prolylmethyl>-N-isopropylcarbamate

There total 2 articles about p-nitrophenyl N-<<<6-(N-BOC-amino)hexyl>succinamido>-L-alanyl-L-alanyl-L-prolylmethyl>-N-isopropylcarbamate 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:

: 65915-94-8
N-(tert-butoxycarbonyl)-1,6-diaminohexane hydrochloride

: 157801-10-0
p-nitrophenyl N-<<<6-(N-BOC-amino)hexyl>succinamido>-L-alanyl-L-alanyl-L-prolylmethyl>-N-isopropylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / triethylamine (TEA) / acetonitrile / 0.5 h

2: 1.) NMN, isobutyl chloroformate / 1.) THF, -20 deg C, 15 min, 2.) THF, from -20 deg C to RT, 5 h

With nicotinamide mononucleotide; triethylamine; isobutyl chloroformate; In acetonitrile;
DOI:10.1021/jm00038a014

Reference yield:

: 157801-09-7
1-(N-t-BOC-amino)-6-hemisuccinamidohexane

: (2-{(S)-1-[(S)-2-((S)-2-Amino-propionylamino)-propionyl]-pyrrolidin-2-yl}-2-oxo-ethyl)-isopropyl-carbamic acid 4-nitro-phenyl ester; hydrochloride

: 157801-10-0
p-nitrophenyl N-<<<6-(N-BOC-amino)hexyl>succinamido>-L-alanyl-L-alanyl-L-prolylmethyl>-N-isopropylcarbamate

Guidance literature:: With nicotinamide mononucleotide; isobutyl chloroformate; Yield given. Multistep reaction; 1.) THF, -20 deg C, 15 min, 2.) THF, from -20 deg C to RT, 5 h;
DOI:10.1021/jm00038a014