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"2-({[(2,4-dimethylphenyl)carbonyl]carbamothioyl}amino)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide" is a complex organic compound with a molecular formula of C20H22N2O2S2. It is characterized by a benzothiophene core, which is a sulfur-containing aromatic ring system. The compound features a carbamoylthioyl group attached to the 2-position of the benzothiophene, and a 2,4-dimethylphenylcarbonyl group, which is a derivative of benzoic acid with two methyl groups at the 2 and 4 positions. This structure contributes to the compound's chemical properties and potential applications, which may include pharmaceutical or chemical research contexts. The compound's specific role or use is not detailed in the provided information, but its structure suggests it could be involved in various chemical or biological interactions due to its diverse functional groups.

5728-37-0

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5728-37-0 Usage

Molecular structure

The compound has a benzothiophene ring system, a carbamothioyl group, and a carboxamide group attached to it.

Substituents

The compound contains a 2,4-dimethylphenyl group, which is a phenyl group with two methyl groups attached at the 2nd and 4th positions.

Complexity

The compound is a complex organic molecule with multiple functional groups and a heterocyclic ring system.

Potential applications

The compound has potential uses in pharmaceuticals and agrochemicals due to its structural features and possible biological activity.

Research necessity

Further research and study are needed to fully understand the compound's properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5728-37-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,2 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5728-37:
(6*5)+(5*7)+(4*2)+(3*8)+(2*3)+(1*7)=110
110 % 10 = 0
So 5728-37-0 is a valid CAS Registry Number.

5728-37-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2,4-dimethylbenzoyl)carbamothioylamino]-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide

1.2 Other means of identification

Product number -
Other names 2-Chlor-4-cyan-biphenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5728-37-0 SDS

5728-37-0Downstream Products

5728-37-0Relevant articles and documents

A fragment-based approach leading to the discovery of a novel binding site and the selective CK2 inhibitor CAM4066

De Fusco, Claudia,Brear, Paul,Iegre, Jessica,Georgiou, Kathy Hadje,Sore, Hannah F.,Hyv?nen, Marko,Spring, David R.

supporting information, p. 3471 - 3482 (2017/05/29)

Recently we reported the discovery of a potent and selective CK2α inhibitor CAM4066. This compound inhibits CK2 activity by exploiting a pocket located outside the ATP binding site (αD pocket). Here we describe in detail the journey that led to the discov

Silver-catalyzed arylation of (hetero)arenes by oxidative decarboxylation of aromatic carboxylic acids

Kan, Jian,Huang, Shijun,Lin, Jin,Zhang, Min,Su, Weiping

supporting information, p. 2199 - 2203 (2015/02/19)

A long-standing challenge in Minisci reactions is achieving the arylation of heteroarenes by oxidative decarboxylation of aromatic carboxylic acids. To address this challenge, the silver-catalyzed intermolecular Minisci reaction of aromatic carboxylic acids was developed. With an inexpensive silver salt as a catalyst, this new reaction enables a variety of aromatic carboxylic acids to undergo decarboxylative coupling with electron-deficient arenes or heteroarenes regardless of the position of the substituents on the aromatic carboxylic acid, thus eliminating the need for ortho-substituted aromatic carboxylic acids, which were a limitation of previously reported methods.

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