methyl N-(4-butylphenyl)carbamate

Base Information

Chemical Name:methyl N-(4-butylphenyl)carbamate
CAS No.:113932-84-6
Molecular Formula:C12H17NO2
Molecular Weight:0.00000
Hs Code.:
DSSTox Substance ID:DTXSID00876909
Nikkaji Number:J1.558.798I
Wikidata:Q82858635
ChEMBL ID:CHEMBL1406856
Mol file:113932-84-6.mol

Synonyms:methyl N-(4-butylphenyl)carbamate;methyl 4-butylphenylcarbamate;113932-84-6;SMR000109763;Cambridge id 7291421;MLS000113873;SCHEMBL2088667;methyl (4-butylphenyl)carbamate;CHEMBL1406856;DTXSID00876909;HMS1591M13;HMS2172I18;STK433684;AKOS003290828;(4-Butylphenyl)carbamic acid methyl ester;Carbamic acid, (4-butylphenyl)-, methyl ester;AK-968/41820585;SR-01000257705;SR-01000257705-1

Suppliers and Price of methyl N-(4-butylphenyl)carbamate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 0 raw suppliers

Chemical Property of methyl N-(4-butylphenyl)carbamate

Chemical Property:

PSA：0.00000
LogP:0.00000
XLogP3:3.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:207.125928785
Heavy Atom Count:15
Complexity:186

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCC1=CC=C(C=C1)NC(=O)OC

Technology Process of methyl N-(4-butylphenyl)carbamate

There total 1 articles about methyl N-(4-butylphenyl)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: 82.0%

: 67-56-1
methanol

: 107377-07-1
4-n-butylbenzamide

: 113932-84-6
methyl (4-butylphenyl)carbamate

Guidance literature:: With sodium bromide; In acetonitrile; at 50 ℃; for 6h; Electrochemical reaction; Green chemistry;
DOI:10.1039/c8ob01059e