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457-82-9

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457-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 457-82-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 457-82:
(5*4)+(4*5)+(3*7)+(2*8)+(1*2)=79
79 % 10 = 9
So 457-82-9 is a valid CAS Registry Number.

457-82-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-fluorophenyl)-3-(1,3-thiazol-2-yl)thiourea

1.2 Other means of identification

Product number -
Other names HMS2694H04

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:457-82-9 SDS

457-82-9Downstream Products

457-82-9Relevant articles and documents

Antimicrobial and anti-biofilm activity of thiourea derivatives incorporating a 2-aminothiazole scaffold

Stefanska, Joanna,Nowicka, Grazyna,Struga, Marta,Szulczyk, Daniel,Koziol, Anna Eugenia,Augustynowicz-Kopec, Ewa,Napiorkowska, Agnieszka,Bielenica, Anna,Filipowski, Wojciech,Filipowska, Anna,Drzewiecka, Aleksandra,Giliberti, Gabriele,Madeddu, Silvia,Boi, Stefano,Colla, Paolo La,Sanna, Giuseppina

, p. 225 - 236 (2015/03/18)

A series of new thiourea derivatives of 1,3-thiazole have been synthesized. All obtained compounds were tested in vitro against a number of microorganisms, including Gram-positive cocci, Gram-negative rods and Candida albicans . Compounds were also tested for their in vitro tuberculostatic activity against the Mycobacterium tuberculosis H37Rv strain, as well as two 'wild' strains isolated from tuberculosis patients. Compounds 3 and 9 showed significant inhibition against Gram-positive cocci (standard strains and hospital strain). The range of MIC values is 2-32 μg/mL. Products 3 and 9 effectively inhibited the biofilm formation of both methicillin-resistant and standard strains of S. epidermidis. The halogen atom, especially at the 3rd position of the phenyl group, is significantly important for this antimicrobial activity. Moreover, all obtained compounds resulted in cytotoxicity and antiviral activity on a large set of DNA and RNA viruses, including Human Immunodeficiency Virus type 1 (HIV-1) and other several important human pathogens. Compound 4 showed activity against HIV-1 and Coxsackievirus type B5. Seven compounds resulted in cytotoxicity against MT-4 cells (CC5010 μM).

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