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50892-49-4

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50892-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50892-49-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,9 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50892-49:
(7*5)+(6*0)+(5*8)+(4*9)+(3*2)+(2*4)+(1*9)=134
134 % 10 = 4
So 50892-49-4 is a valid CAS Registry Number.

50892-49-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-((4,6-dihydroxypyrimidin-2-yl)thio)acetate

1.2 Other means of identification

Product number -
Other names (4,6-dioxo-1,4,5,6-tetrahydro-pyrimidin-2-ylsulfanyl)-acetic acid ethyl ester

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:50892-49-4 SDS

50892-49-4Relevant articles and documents

Molecular determinants for improved activity at PPARα: Structure-activity relationship of pirinixic acid derivatives, docking study and site-directed mutagenesis of PPARα

Lamers, Christina,Dittrich, Michaela,Steri, Ramona,Proschak, Ewgenij,Schubert-Zsilavecz, Manfred

, p. 4048 - 4052 (2014)

Peroxisome proliferator-activated receptors (PPARs) are attractive targets for the treatment of the metabolic syndrome. Especially a combination of PPARα and PPARγ agonistic activity seems worthwhile to be pursued. Herein we present the design and synthes

Molecular determinants for improved activity at PPARα: Structure-activity relationship of pirinixic acid derivatives, docking study and site-directed mutagenesis of PPARα

Lamers, Christina,Dittrich, Michaela,Steri, Ramona,Proschak, Ewgenij,Schubert-Zsilavecz, Manfred

supporting information, p. 4048 - 4052 (2015/03/14)

Peroxisome proliferator-activated receptors (PPARs) are attractive targets for the treatment of the metabolic syndrome. Especially a combination of PPARα and PPARγ agonistic activity seems worthwhile to be pursued. Herein we present the design and synthes

Design, synthesis, and biological evaluation of a novel class of γ-secretase modulators with pparγ activity

Hieke, Martina,Ness, Julia,Steri, Ramona,Dittrich, Michaela,Greiner, Christine,Werz, Oliver,Baumann, Karlheinz,Schubert-Zsilavecz, Manfred,Weggen, Sascha,Zettl, Heiko

supporting information; experimental part, p. 4691 - 4700 (2010/10/03)

We present a novel class of dual modulators of γ-secretase and peroxisome proliferator-activated receptor γ (PPARγ) based on the structure of 2-(bis(phenethoxy)pyrimidine-2-ylthio)hexanoic acid 8 (IC 50(Aβ42) = 22.8 μM, EC50(PPARγ) =

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