Ethyl (1,3-thiazol-2-ylamino)carbonothioylcarbamate

Base Information

Chemical Name:Ethyl (1,3-thiazol-2-ylamino)carbonothioylcarbamate
CAS No.:39142-41-1
Molecular Formula:C₇H₉N₃O₂S₂
Molecular Weight:231.299
Hs Code.:
DSSTox Substance ID:DTXSID301235326
Mol file:39142-41-1.mol

Synonyms:39142-41-1;ethyl (1,3-thiazol-2-ylamino)carbonothioylcarbamate;ethyl N-[(1,3-thiazol-2-yl)carbamothioyl]carbamate;Ethyl (1,3-thiazol-2-ylcarbamothioyl)carbamate;ethyl N-(1,3-thiazol-2-ylcarbamothioyl)carbamate;DTXSID301235326;AKOS009149026;CS-0244795;EN300-29427;Ethyl(1,3-thiazol-2-ylcarbamothioyl)carbamate;Ethyl N-[(2-thiazolylamino)thioxomethyl]carbamate;Z283724538;Carbamic acid, [(2-thiazolylamino)thioxomethyl]-, ethyl ester (9CI)

Suppliers and Price of Ethyl (1,3-thiazol-2-ylamino)carbonothioylcarbamate

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

TRC
EthylN-[(1,3-Thiazol-2-yl)carbamothioyl]carbamate
50mg
$ 90.00

Total 5 raw suppliers

Chemical Property of Ethyl (1,3-thiazol-2-ylamino)carbonothioylcarbamate

Chemical Property:

Melting Point:166-167 °C(Solv: ethanol (64-17-5))
PKA:6.07±0.70(Predicted)
PSA：123.58000
Density:1.460±0.06 g/cm3(Predicted)
LogP:2.04990
XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:231.01361889
Heavy Atom Count:14
Complexity:225

Purity/Quality:

99% ^*data from raw suppliers

EthylN-[(1,3-Thiazol-2-yl)carbamothioyl]carbamate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)NC(=S)NC1=NC=CS1

Technology Process of Ethyl (1,3-thiazol-2-ylamino)carbonothioylcarbamate

There total 1 articles about Ethyl (1,3-thiazol-2-ylamino)carbonothioylcarbamate 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:

: 96-50-4
2-thiazolylamine

: 16182-04-0
Ethoxycarbonyl isothiocyanate

: 39142-41-1
ethyl (1,3-thiazol-2-ylcarbamothioyl)carbamate

Guidance literature:: In ethyl acetate;

Reference yield:

: 39142-41-1
ethyl (1,3-thiazol-2-ylcarbamothioyl)carbamate

: 37663-61-9
2-benzylsulfanyl-thiazolo[3,2-a][1,3,5]triazin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / acetone

2: 160 - 170 °C / 80 Torr

With potassium carbonate; In acetone;