Benzyl propylcarbamate

Base Information

Chemical Name:Benzyl propylcarbamate
CAS No.:65095-17-2
Molecular Formula:C₁₁H₁₅NO₂
Molecular Weight:193.246
Hs Code.:
DSSTox Substance ID:DTXSID101306379
Nikkaji Number:J306.014D

Synonyms:benzyl propylcarbamate;benzyl N-propylcarbamate;65095-17-2;Phenylmethyl N-propylcarbamate;SCHEMBL733157;Propylcarbamic acid benzyl ester;CSOLJDWYEPDGKF-UHFFFAOYSA-N;DTXSID101306379;FT-0749223

Suppliers and Price of Benzyl propylcarbamate

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 2 raw suppliers

Chemical Property of Benzyl propylcarbamate

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:193.110278721
Heavy Atom Count:14
Complexity:165

Purity/Quality:: 99% ，98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCNC(=O)OCC1=CC=CC=C1

Technology Process of Benzyl propylcarbamate

There total 17 articles about Benzyl propylcarbamate 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: 100.0%

: 5041-33-8
N-(Benzyloxycarbonyl)allylamine

: 65095-17-2
N-(benzyloxycarbonyl)propylamine

Guidance literature:: With hydrazine hydrate; In ethanol; for 24h; Reflux;
DOI:10.1139/v2012-057

Reference yield: 97.0%

: 556-53-6
N-propylamine hydrochloride

: 91806-74-5
3,5-dimethyl-pyrazole-1-carboxylic acid benzyl ester

: 65095-17-2
N-(benzyloxycarbonyl)propylamine

Guidance literature:: With triethylamine; In tetrahydrofuran; at 60 ℃; for 5.5h;
DOI:10.1016/S0040-4020(98)00947-8

Reference yield: 94.0%

: 621-84-1
O-benzyl carbamate

: 123-38-6
propionaldehyde

: 65095-17-2
N-(benzyloxycarbonyl)propylamine

Guidance literature:: With triethylsilane; perrhenic acid anhydride; In dichloromethane; at 20 ℃; for 0.5h; chemoselective reaction;
DOI:10.1039/c2cc33185c