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57206-73-2

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57206-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57206-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,0 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57206-73:
(7*5)+(6*7)+(5*2)+(4*0)+(3*6)+(2*7)+(1*3)=122
122 % 10 = 2
So 57206-73-2 is a valid CAS Registry Number.

57206-73-2SDS

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 1,3-bis-(4-chloro-benzyl)-thiourea

1.2 Other means of identification

Product number -
Other names N,N'-Bis-(4-chlor-benzyl)-thioharnstoff

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:57206-73-2 SDS

57206-73-2Relevant articles and documents

New potent imidazoisoquinolinone derivatives as anti-Trypanosoma cruzi agents: Biological evaluation and structure-activity relationships

Bollini, Mariela,Casal, Juan Jose,Alvarez, Diego E.,Boiani, Lucia,Gonzalez, Mercedes,Cerecetto, Hugo,Bruno, Ana Maria

experimental part, p. 1437 - 1444 (2009/09/25)

A series of novel benzoimidazo and N-aryl-5-oxo-imidazo[1,2-b]isoquinoline-10-carbothioamides was developed. All the compounds were evaluated for their in vitro action against the epimastigote form of Trypanosoma cruzi. Four of them showed higher activity than Nifurtimox. Their unspecific cytotoxicity was evaluated using HeLa and L6 cells, being non-toxic at concentrations at least 15 and 200 times higher than that of T. cruzi IC50. To gain insight into the mechanism of action, their DNA binding properties and reactivity with glutathione were studied, and QSAR study was performed.

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