benzyl N-[2-[[1-hydrazinyl-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-2-oxoethyl]carbamate

Base Information

Chemical Name:benzyl N-[2-[[1-hydrazinyl-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-2-oxoethyl]carbamate
CAS No.:17682-11-0
Molecular Formula:C₁₆H₂₀N₆O₄
Molecular Weight:360.373
Hs Code.:
NSC Number:118511
Mol file:17682-11-0.mol

Synonyms:benzyl N-[2-[[1-hydrazinyl-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-2-oxoethyl]carbamate;17682-11-0;NSC118511;NSC-118511

Suppliers and Price of benzyl N-[2-[[1-hydrazinyl-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-2-oxoethyl]carbamate

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
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price

Total 7 raw suppliers

Chemical Property of benzyl N-[2-[[1-hydrazinyl-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-2-oxoethyl]carbamate

Chemical Property:

Vapor Pressure:1.69E-28mmHg at 25°C
Boiling Point:840.8°Cat760mmHg
Flash Point:462.3°C
PSA：151.23000
Density:1.358g/cm³
LogP:1.22630
Storage Temp.:-15°C
XLogP3:-0.5
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:9
Exact Mass:360.15460314
Heavy Atom Count:26
Complexity:483

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)NCC(=O)NC(CC2=CN=CN2)C(=O)NN

Technology Process of benzyl N-[2-[[1-hydrazinyl-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-2-oxoethyl]carbamate

There total 2 articles about benzyl N-[2-[[1-hydrazinyl-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-2-oxoethyl]carbamate 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:

: 50622-95-2
benzyl (2-azido-2-oxoethyl)carbamate

: 1499-46-3
L-Histidine methyl ester

: 17682-11-0
N^α-(N-benzyloxycarbonyl-glycyl)-histidine hydrazide

Guidance literature:: With chloroform; und anschliessendes Behandeln mit N₂H₄;
DOI:10.1021/ja01649a019

Reference yield:

: 17682-11-0
N^α-(N-benzyloxycarbonyl-glycyl)-histidine hydrazide

Guidance literature:: Histidin-methylester-hydrochlorid, 1. CHCl3, Z-Gly, 2. Dicyclohexylcarbodiimid, 3. Hydrazinhydrat;

Reference yield:

: 17682-11-0
N^α-(N-benzyloxycarbonyl-glycyl)-histidine hydrazide

: 89032-50-8
[(S)-2-[(S)-2-(2-Benzyloxycarbonylamino-acetylamino)-3-(1H-imidazol-4-yl)-propionylamino]-3-(1H-indol-3-yl)-propionylamino]-acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: NaNO₂

2: 1N NaOH, 1N HCl / methanol / 1 h / Ambient temperature

With hydrogenchloride; sodium hydroxide; sodium nitrite; In methanol;
DOI:10.1021/j150653a021