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Carbamic acid, (chlorothio)methyl-, butyl ester

Base Information Edit
  • Chemical Name:Carbamic acid, (chlorothio)methyl-, butyl ester
  • CAS No.:64831-38-5
  • Molecular Formula:C6H12ClNO2S
  • Molecular Weight:197.686
  • Hs Code.:
  • Mol file:64831-38-5.mol
Carbamic acid, (chlorothio)methyl-, butyl ester

Synonyms:N-Methyl-N-chlorthio-n-butylcarbamat;n-butyl N-chlorothio-N-methylcarbamate;

Suppliers and Price of Carbamic acid, (chlorothio)methyl-, butyl ester
Supply Marketing:Edit
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
  • TRC
  • ButylN-(Chlorosulfenyl)-N-methylcarbamate
  • 50mg
  • $ 345.00
Total 0 raw suppliers
Chemical Property of Carbamic acid, (chlorothio)methyl-, butyl ester Edit
Chemical Property:
  • PSA:67.12000 
  • LogP:2.56160 
Purity/Quality:

ButylN-(Chlorosulfenyl)-N-methylcarbamate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Butyl N-(Chlorosulfenyl)-N-methylcarbamate is an intermediate in synthesizing Furathiocarb (F863780), a pesticide.
Technology Process of Carbamic acid, (chlorothio)methyl-, butyl ester

There total 1 articles about Carbamic acid, (chlorothio)methyl-, 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:
Guidance literature:
N-Methyl-n-butylcarbamat, SCl2;
DOI:10.1021/jf60217a021
Guidance literature:
With sodium hydride; In tetrahydrofuran; (N2); addn. of NaH to a soln. of iron complex in THF, stirring at room temp. for 0.5 h, cooling to 0°C, addn. of a soln. of carbamate in THF, stirring for 8 h at room temp.; filtration, concn., column chromy (SiO2, petroleum ether/ethyl acetate);elem. anal.;
DOI:10.1016/S0022-328X(01)00876-2
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