Carbamic acid, 3-chlorophenyl-, butyl ester

Base Information

Chemical Name:Carbamic acid, 3-chlorophenyl-, butyl ester
CAS No.:2445-41-2
Molecular Formula:C11H14ClNO2
Molecular Weight:227.691
Hs Code.:
DSSTox Substance ID:DTXSID50423664
Nikkaji Number:J3.116.235A
Wikidata:Q82235918
Mol file:2445-41-2.mol

Synonyms:2445-41-2;Carbamic acid, 3-chlorophenyl-, butyl ester;Carbamic acid, (3-chlorophenyl)-, butyl ester;SCHEMBL11218133;DTXSID50423664;BNTSUNVFPLPWCD-UHFFFAOYSA-N;AKOS002963790;N-(3-Chlorophenyl)carbamic acid butyl ester

Suppliers and Price of Carbamic acid, 3-chlorophenyl-, butyl ester

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 1 raw suppliers

Chemical Property of Carbamic acid, 3-chlorophenyl-, butyl ester

Chemical Property:

XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:227.0713064
Heavy Atom Count:15
Complexity:199

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCOC(=O)NC1=CC(=CC=C1)Cl

Technology Process of Carbamic acid, 3-chlorophenyl-, butyl ester

There total 4 articles about Carbamic acid, 3-chlorophenyl-, butyl ester 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: 80.0%

: 590-28-3
potassium cyanate

: 108-37-2
1-bromo-3-chlorobenzene

: 71-36-3
butan-1-ol

: 2445-41-2
butyl 3-chlorophenylcarbamate

Guidance literature:: With copper(l) iodide; 2-(2,6-dimethylphenyl-amino)-2-oxoacetic acid potassium salt; at 110 ℃; for 24h; Inert atmosphere;
DOI:10.1002/adsc.201200296

Reference yield: 75.0%

: 590-28-3
potassium cyanate

: 625-99-0
3-iodochlorobenzene

: 71-36-3
butan-1-ol

: 2445-41-2
butyl 3-chlorophenylcarbamate

Guidance literature:: With copper(l) iodide; 2-(2,6-dimethylphenyl-amino)-2-oxoacetic acid potassium salt; at 100 ℃; for 24h; Inert atmosphere;
DOI:10.1002/adsc.201200296