p-Nitrophenyl N2-(benzyloxycarbonyl)-L-lysinate

Base Information

Chemical Name:p-Nitrophenyl N2-(benzyloxycarbonyl)-L-lysinate
CAS No.:4272-71-3
Molecular Formula:C20H23N3O6
Molecular Weight:401.419
Hs Code.:2924299090
European Community (EC) Number:224-265-9
DSSTox Substance ID:DTXSID50962649
Nikkaji Number:J205.679H
Wikidata:Q82944357

Synonyms:alpha-Cbz-lysine-p-nitrophenyl ester;alpha-N-benzyloxycarbonyl-L-lysine para-nitrophenyl ester;CbzLNP;N-(alpha)-carbobenzoxylysine-4-nitrophenyl ester;N-benzyloxycarbonyllysine 4-nitrophenyl ester;N-benzyloxycarbonyllysine 4-nitrophenyl ester hydrochloride;Z-Lys-Nph

Suppliers and Price of p-Nitrophenyl N2-(benzyloxycarbonyl)-L-lysinate

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 8 raw suppliers

Chemical Property of p-Nitrophenyl N2-(benzyloxycarbonyl)-L-lysinate

Chemical Property:

Vapor Pressure:1.2E-14mmHg at 25°C
Melting Point:150-152oC
Boiling Point:606.3°Cat760mmHg
PKA:10.61±0.46(Predicted)
Flash Point:320.5°C
PSA：38.69000
Density:1.274g/cm³
LogP:0.42030
Storage Temp.:?20°C
XLogP3:2.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:11
Exact Mass:401.15868546
Heavy Atom Count:29
Complexity:525

Purity/Quality:: 98%Min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC(=O)NC(CCCCN)C(=O)OC2=CC=C(C=C2)[N+](=O)[O-]
Isomeric SMILES:C1=CC=C(C=C1)COC(=O)N[C@@H](CCCCN)C(=O)OC2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of p-Nitrophenyl N2-(benzyloxycarbonyl)-L-lysinate

There total 1 articles about p-Nitrophenyl N2-(benzyloxycarbonyl)-L-lysinate 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:

: 2212-69-3
N₂-benzyloxycarbonyl-N₆-t-butoxycarbonyl-L-lysine 4-nitrophenyl ester

: 4272-71-3
N^α-benzyloxycarbonyl-L-lysine p-nitrophenyl ester

Guidance literature:: With hydrogenchloride;
DOI:10.1021/ja00976a034

Reference yield: 86.0%

: 87-51-4
indole-3-acetic acid

: 4272-71-3
N^α-benzyloxycarbonyl-L-lysine p-nitrophenyl ester

: 150151-61-4
N-α-Carbobenzyloxy-N-ε-(indole-3-acetyl)-L-lysine-p-nitrophenylester

Guidance literature:: With pyridine; dicyclohexyl-carbodiimide; In chloroform; for 3.5h; Ambient temperature;
DOI:10.1016/0031-9422(93)85388-8

Reference yield:

: 4272-71-3
N^α-benzyloxycarbonyl-L-lysine p-nitrophenyl ester

: 100-02-7,78813-13-5,89830-32-0
4-nitro-phenol

: 2212-75-1
N₂-[(benzyloxy)carbonyl]-L-lysine

Guidance literature:: With water; at 21 ℃; Kinetics; Thermodynamic data; Mechanism; pH dependence of the rate constant and catalytic effect of amino acid, E(act.), ΔS(excit.);