1915-80-6 Usage
Uses
Used in Pharmaceutical Industry:
2-Methyl-3-(2,4-dimethylphenyl)quinazolin-4(3H)-one is used as a pharmaceutical compound for its potential therapeutic properties. The compound may exhibit biological activities that can be harnessed for the development of new drugs, particularly in the treatment of various diseases and disorders.
Used in Chemical Research:
In the field of chemical research, 2-Methyl-3-(2,4-dimethylphenyl)quinazolin-4(3H)-one serves as a valuable compound for studying the structure-activity relationships of quinazolinone derivatives. It can be used as a starting material or a reference compound in the synthesis and evaluation of new quinazolinone-based molecules with improved or novel biological activities.
Used in Material Science:
2-Methyl-3-(2,4-dimethylphenyl)quinazolin-4(3H)-one may also find applications in material science, particularly in the development of new organic materials with specific properties. The compound's unique structure and potential for functionalization can be exploited to create materials with tailored characteristics for various applications, such as in electronics, optics, or sensing technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 1915-80-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1915-80:
(6*1)+(5*9)+(4*1)+(3*5)+(2*8)+(1*0)=86
86 % 10 = 6
So 1915-80-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H16N2O/c1-11-8-9-16(12(2)10-11)19-13(3)18-15-7-5-4-6-14(15)17(19)20/h4-10H,1-3H3
1915-80-6Relevant academic research and scientific papers
Metal-free C-H methylation and acetylation of heteroarenes with PEG-400
Kudale, Vishal Suresh,Wang, Jeh-Jeng
supporting information, p. 3506 - 3511 (2020/06/25)
The generation of a methyl carbon source from renewable and cheap sources is challenging. Herein, we describe a novel and an efficient route for methylation and acetylation of aza-heteroarenes using PEG-400 under O2and TsOH·H2O for the first time by tuning the reaction conditions using a different set of starting materials. The key features of the current protocol are oxidative C-O and C-C bond scission under metal-free conditions with good functional group tolerance, and a broad substrate scope. The potential applicability of the designed methodology was demonstrated for the synthesis of central nervous system (CNS) depressant and anticonvulsant drug molecules by a one-pot strategy.
Compounds for modulating TRPV3 function
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Page/Page column 52, (2010/11/28)
The present application relates to compounds and methods for treating pain and other conditions related to TRPV3.
