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583-46-0

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583-46-0 Usage

Description

(5E)-5-benzylidene-2-sulfanylidene-imidazolidin-4-one is a heterocyclic organic compound characterized by a molecular formula of C11H11NOS. It features a five-membered ring that incorporates both sulfur and nitrogen atoms, which may contribute to its potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
(5E)-5-benzylidene-2-sulfanylidene-imidazolidin-4-one is used as a chemical compound for its potential pharmaceutical applications. Its unique structure and possible biological activities make it a candidate for further research and development in the creation of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, (5E)-5-benzylidene-2-sulfanylidene-imidazolidin-4-one is used as a chemical compound for its potential to be developed into new agrochemical products. Its specific properties may be harnessed for applications such as pesticides or fertilizers, contributing to agricultural productivity and crop protection.
Safety and Handling:
It is important to handle (5E)-5-benzylidene-2-sulfanylidene-imidazolidin-4-one with care, as it may have specific safety and handling guidelines. Due to its potential reactivity and toxicity, proper precautions should be taken to ensure the safety of those working with this compound in both research and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 583-46-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 583-46:
(5*5)+(4*8)+(3*3)+(2*4)+(1*6)=80
80 % 10 = 0
So 583-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2OS/c13-9-8(11-10(14)12-9)6-7-4-2-1-3-5-7/h1-6H,(H2,11,12,13,14)/b8-6+

583-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-benzylidene-2-sulfanylideneimidazolidin-4-one

1.2 Other means of identification

Product number -
Other names 5-benzal-2-thiohydantoin

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:583-46-0 SDS

583-46-0Relevant articles and documents

Bioisosteric modification of known fucosidase inhibitors to discover a novel inhibitor of α-l-fucosidase

Bathula, Chandramohan,Ghosh, Shreemoyee,Hati, Santanu,Tripathy, Sayantan,Singh, Shailja,Chakrabarti, Saikat,Sen, Subhabrata

, p. 3563 - 3572 (2017/01/25)

Bioisosteric modification of known fucosidase inhibitors A and B, resulted in three new types of molecules, 4b, 5c and 6a (belonging to furopyridinedione, thiohydantoin and hydantoin chemotypes) that could potentially bind to α-l-fucosidase (bovine kidney

Design and Synthesis of Novel Phenylpiperazine Derivatives as Potential Anticonvulsant Agents

Habib, Monica M. W.,Abdelfattah, Mohamed A. O.,Abadi, Ashraf H.

, p. 868 - 874 (2015/12/24)

Eighteen new 5-benzylidene-3-(4-arylpiperazin-1-ylmethyl)-2-thioxo-imidazolidin-4-ones were designed as hybrid structures from previously reported anticonvulsant compounds, synthesized and tested for anticonvulsant activity. Initial anticonvulsant screeni

SYNTHESIS OF IMIDAZOLE-2-THIONES VIA THIOHYDANTOINS

-

Page/Page column 33, (2010/11/26)

The present invention provides a method of making an imidazole 2-thione which comprises the step(s) of reducing a thiohydantoin to said imidazole- 2-thione.

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