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Benzenamine, 4-[4-(methylsulfonyl)-6-(2-thienyl)-2-pyrimidinyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

832075-88-4

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832075-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 832075-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,2,0,7 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 832075-88:
(8*8)+(7*3)+(6*2)+(5*0)+(4*7)+(3*5)+(2*8)+(1*8)=164
164 % 10 = 4
So 832075-88-4 is a valid CAS Registry Number.

832075-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-methylsulfonyl-6-thiophen-2-ylpyrimidin-2-yl)aniline

1.2 Other means of identification

Product number -
Other names -

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:832075-88-4 SDS

832075-88-4Downstream Products

832075-88-4Relevant academic research and scientific papers

Syntheses of 2,4,6-trisubstituted pyrimidine derivatives as a new class of antifilarial topoisomerase II inhibitors

Katiyar, Sanjay Babu,Bansal, Iti,Saxena,Chauhan

, p. 47 - 50 (2007/10/03)

A series of 21 compounds of trisubstituted pyrimidine derivatives have been synthesized and evaluated for their in vitro topoisomerase II inhibitory activity against filarial parasite Setaria cervi. Out of these, five compounds (12, 13, 14, 25 and 28) exhibited 70-80% inhibition at 10 μg/mL and three compounds (13, 14 and 28) have shown 40-60% inhibition at 5 μg/mL concentration. A series of 21 compounds of trisubstituted pyrimidine derivatives have been synthesized and evaluated for their in vitro topoisomerase II inhibitory activity against filarial parasite Setaria cervi. Out of these, seven compounds (8, 11-14, 25 and 28) have shown 60-80% inhibition at 40 and 20 μg/mL concentration. Five compounds (12, 13, 14, 25 and 28) exhibited 70-80% inhibition at 10 μg/mL concentration and three compounds (13, 14 and 28) have shown 40-60% inhibition at 5 μg/mL concentration. All the above mentioned compounds have shown better topo II inhibitory activity than standard antifilarial drug (DEC) and enzyme topo II inhibitors (Novobiocin, Nalidixic acid).

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