ethyl N-(phenylcarbamothioylamino)carbamate

Base Information

Chemical Name:ethyl N-(phenylcarbamothioylamino)carbamate
CAS No.:38110-48-4
Molecular Formula:C10H13 N3 O2 S
Molecular Weight:239.2941
Hs Code.:
NSC Number:119342
DSSTox Substance ID:DTXSID60372477
Mol file:38110-48-4.mol

Synonyms:ethyl N-(phenylcarbamothioylamino)carbamate;38110-48-4;NSC119342;Maybridge1_008473;HMS565J03;DTXSID60372477;CCG-254560;NSC-119342

Suppliers and Price of ethyl N-(phenylcarbamothioylamino)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
Packaging
price

Total 4 raw suppliers

Chemical Property of ethyl N-(phenylcarbamothioylamino)carbamate

Chemical Property:

Density:1.296g/cm³
XLogP3:1.8
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:239.07284784
Heavy Atom Count:16
Complexity:242

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)NNC(=S)NC1=CC=CC=C1

Technology Process of ethyl N-(phenylcarbamothioylamino)carbamate

There total 9 articles about ethyl N-(phenylcarbamothioylamino)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:

: 62-53-3
aniline

: 38110-48-4
3-phenylthiocarbamoyl-carbazic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 1 h / 25 °C

2: tetrahydrofuran / 2 h / Reflux

With triethylamine; In tetrahydrofuran;
DOI:10.2478/s11696-012-0228-1