N-(cyclohexylcarbamothioyl)benzamide

Base Information

Chemical Name:N-(cyclohexylcarbamothioyl)benzamide
CAS No.:4921-92-0
Molecular Formula:C14H18N2OS
Molecular Weight:262.376
Hs Code.:
European Community (EC) Number:812-984-6
DSSTox Substance ID:DTXSID70884117
Nikkaji Number:J1.472.375G
Wikidata:Q82862857
ChEMBL ID:CHEMBL1555726
Mol file:4921-92-0.mol

Synonyms:N-(cyclohexylcarbamothioyl)benzamide;4921-92-0;3-benzoyl-1-cyclohexylthiourea;CHEMBL1555726;Benzamide, N-[(cyclohexylamino)thioxomethyl]-;Benzamide, N-((cyclohexylamino)thioxomethyl)-;MLS001034907;1-Benzoyl-3-cyclohexylthiourea;SCHEMBL16108484;DTXSID70884117;N-benzoyl N'-cyclohexyl thiourea;BDBM50443480;STK133453;AKOS003422788;SMR000665372;CS-0368014;2N-014

Suppliers and Price of N-(cyclohexylcarbamothioyl)benzamide

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 2 raw suppliers

Chemical Property of N-(cyclohexylcarbamothioyl)benzamide

Chemical Property:

Melting Point:64 °C
PSA：73.22000
LogP:3.40540
XLogP3:3.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:262.11398438
Heavy Atom Count:18
Complexity:294

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC(CC1)NC(=S)NC(=O)C2=CC=CC=C2

Technology Process of N-(cyclohexylcarbamothioyl)benzamide

There total 6 articles about N-(cyclohexylcarbamothioyl)benzamide 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: 100.0%

: 108-91-8,157973-60-9
cyclohexylamine

: 532-55-8
Benzoyl isothiocyanate

: 4921-92-0
TM-2-97

Guidance literature:: In dichloromethane; at 0 - 20 ℃; for 2h;
DOI:10.1021/ml400412x

Reference yield:

: ammonium thiocyanate

: 108-91-8,157973-60-9
cyclohexylamine

: 98-88-4
benzoyl chloride

: 4921-92-0
TM-2-97

Guidance literature:: ammonium thiocyanate; benzoyl chloride; In acetone; for 0.25h; Reflux;

cyclohexylamine; In acetone; for 0.5h; Reflux;
DOI:10.1016/j.tetlet.2015.10.088

Reference yield:

: 98-88-4
benzoyl chloride

: 4921-92-0
TM-2-97

Guidance literature:: Multi-step reaction with 2 steps

1: acetone / 0.5 h / Reflux

2: acetone / 0.5 h / Reflux

In acetone;
DOI:10.1016/j.bmcl.2011.07.080