112559-69-0 Usage
Description
2-[2-(3-OXOBUTYL)]-4-4-[4-(4-HYDROXYPHENYL)-PIPERAZIN-1-YL]-PHENYL-2,4-DIHYDRO-[1,2,4-TRIAZOL-3-ONE (CAS# 112559-69-0) is a complex organic compound with a unique molecular structure. It is characterized as an off-white solid and is primarily used in organic synthesis due to its versatile chemical properties.
Uses
1. Used in Organic Synthesis:
2-[2-(3-OXOBUTYL)]-4-4-[4-(4-HYDROXYPHENYL)-PIPERAZIN-1-YL]-PHENYL-2,4-DIHYDRO-[1,2,4-TRIAZOL-3-ONE is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with different functional groups, making it a valuable asset in the field of organic chemistry.
2. Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-[2-(3-OXOBUTYL)]-4-4-[4-(4-HYDROXYPHENYL)-PIPERAZIN-1-YL]-PHENYL-2,4-DIHYDRO-[1,2,4-TRIAZOL-3-ONE is utilized as a building block for the development of new drugs. Its chemical properties enable the creation of molecules with potential therapeutic applications, contributing to the advancement of medicinal chemistry.
3. Used in Chemical Research:
2-[2-(3-OXOBUTYL)]-4-4-[4-(4-HYDROXYPHENYL)-PIPERAZIN-1-YL]-PHENYL-2,4-DIHYDRO-[1,2,4-TRIAZOL-3-ONE is also employed in chemical research for studying various reaction mechanisms and exploring new synthetic routes. Its unique structure provides researchers with opportunities to investigate novel chemical transformations and develop innovative methodologies in organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 112559-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,5,5 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112559-69:
(8*1)+(7*1)+(6*2)+(5*5)+(4*5)+(3*9)+(2*6)+(1*9)=120
120 % 10 = 0
So 112559-69-0 is a valid CAS Registry Number.
112559-69-0Relevant 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
