N-[(thiophen-2-ylmethyl)carbamothioyl]benzamide

Base Information

Chemical Name:N-[(thiophen-2-ylmethyl)carbamothioyl]benzamide
CAS No.:123403-76-9
Molecular Formula:C₁₃H₁₂N₂OS₂
Molecular Weight:276.383
Hs Code.:
DSSTox Substance ID:DTXSID901232906
ChEMBL ID:CHEMBL1834371

Synonyms:N-[(thiophen-2-ylmethyl)carbamothioyl]benzamide;CHEMBL1834371;SCHEMBL10483464;DTXSID901232906;STK000085;AKOS003453410;N-[[(2-Thienylmethyl)amino]thioxomethyl]benzamide;SR-01000253480;SR-01000253480-1;123403-76-9

Suppliers and Price of N-[(thiophen-2-ylmethyl)carbamothioyl]benzamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of N-[(thiophen-2-ylmethyl)carbamothioyl]benzamide

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:276.03910536
Heavy Atom Count:18
Complexity:303

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)NC(=S)NCC2=CC=CS2

Technology Process of N-[(thiophen-2-ylmethyl)carbamothioyl]benzamide

There total 2 articles about N-[(thiophen-2-ylmethyl)carbamothioyl]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:

: 27757-85-3
2-Aminomethylthiophene

: 532-55-8
Benzoyl isothiocyanate

: 123403-76-9
TM-2-107

Guidance literature:: In chloroform; for 2h; Heating;
DOI:10.1016/j.bmcl.2007.01.081

Reference yield:

: 98-88-4
benzoyl chloride

: 123403-76-9
TM-2-107

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