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250255-72-2

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  • 2-[2-(3-Oxobutyl)]-4-{4-[4-(4-methoxyphenyl)-piperazin-1-yl]-phenyl}-2,4-dihydro-[1,2,4-triazol-3-one

    Cas No: 250255-72-2

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250255-72-2 Usage

Chemical Properties

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Uses

2-[2-(3-Oxobutyl)]-4-{4-[4-(4-methoxyphenyl)-piperazin-1-yl]-phenyl}-2,4-dihydro-[1,2,4-triazol-3-one (cas# 250255-72-2) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 250255-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,0,2,5 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 250255-72:
(8*2)+(7*5)+(6*0)+(5*2)+(4*5)+(3*5)+(2*7)+(1*2)=112
112 % 10 = 2
So 250255-72-2 is a valid CAS Registry Number.

250255-72-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[4-[4-(4-methoxyphenyl)piperazin-1-yl]phenyl]-2-(3-oxobutan-2-yl)-1,2,4-triazol-3-one

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

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More Details:250255-72-2 SDS

250255-72-2Relevant articles and documents

Synthesis and in vitro and in vivo antifungal activity of the hydroxy metabolites of saperconazole

Meerpoel, Lieven,Heeres, Jan,Backx, Leo J. J.,Van Der Veken, Louis J. E.,Hendrickx, Rob,Corens, David,De Groot, Alex,Leurs, Stef,Van Der Eycken, Luc,Weerts, Johan,Luyts, Paul,Van Gerven, Frans,Woestenborghs, Filip A. A.,Van Breda, Andre,Oris, Michel,Van Dorsselaer, Pascal,Willemsens, Gustaaf H. M.,Bellens, Danny,Marichal, Patrick J. M. G.,Vanden Bossche, Hugo F.,Odds, Frank C.

experimental part, p. 757 - 769 (2011/02/23)

Herein we describe the scalable diastereoselective and enantio-selective syntheses of eight enantiomers of hydroxy metabolites of saperconazole. The in vitro antifungal activity of the eight stereoisomers (compounds 1-8) was compared against a broad panel

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