L-Leucyl-N-(4-nitrophenyl)-L-leucinamide

Base Information

Chemical Name:L-Leucyl-N-(4-nitrophenyl)-L-leucinamide
CAS No.:81928-67-8
Molecular Formula:C₁₈H₂₈N₄O₄
Molecular Weight:364.445
Hs Code.:
DSSTox Substance ID:DTXSID30557799
Wikidata:Q82439822

Synonyms:81928-67-8;L-Leucyl-N-(4-nitrophenyl)-L-leucinamide;DTXSID30557799

Suppliers and Price of L-Leucyl-N-(4-nitrophenyl)-L-leucinamide

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 L-Leucyl-N-(4-nitrophenyl)-L-leucinamide

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:364.21105539
Heavy Atom Count:26
Complexity:482

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)CC(C(=O)NC(CC(C)C)C(=O)NC1=CC=C(C=C1)[N+](=O)[O-])N
Isomeric SMILES:CC(C)C[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)NC1=CC=C(C=C1)[N+](=O)[O-])N

Technology Process of L-Leucyl-N-(4-nitrophenyl)-L-leucinamide

There total 3 articles about L-Leucyl-N-(4-nitrophenyl)-L-leucinamide 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: 55.0%

: 123529-88-4
benzyloxycarbonylleucyl-leucine p-nitroanilide

: 81928-67-8
leucyl-leucine p-nitroanilide

Guidance literature:: With hydrogen bromide; In acetic acid; for 1.5h;

Reference yield:

: 2018-66-8
Z-Leu-OH

: 81928-67-8
leucyl-leucine p-nitroanilide

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / DCC / CH₂Cl₂ / 12 h / 3 °C

2: 55 percent / HBr / acetic acid / 1.5 h

With hydrogen bromide; dicyclohexyl-carbodiimide; In dichloromethane; acetic acid;

Reference yield:

: 4178-93-2,110893-28-2,86237-92-5,63324-49-2,6664-98-8
(S)-2-amino-4-methyl-N-(4-nitrophenyl)valeramide

: 81928-67-8
leucyl-leucine p-nitroanilide

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / DCC / CH₂Cl₂ / 12 h / 3 °C

2: 55 percent / HBr / acetic acid / 1.5 h

With hydrogen bromide; dicyclohexyl-carbodiimide; In dichloromethane; acetic acid;