5432-54-2 Usage
Description
(2-methylphenyl)(diphenyl)methanol is a chemical compound that consists of a 2-methylphenyl group and a diphenyl group attached to a methanol molecule. It is known for its potential applications in various fields, including organic chemistry, pharmaceuticals, and agricultural chemicals.
Uses
Used in Organic Chemistry:
(2-methylphenyl)(diphenyl)methanol is used as a building block for creating more complex molecules, contributing to the advancement of organic chemistry.
Used in Pharmaceutical Industry:
(2-methylphenyl)(diphenyl)methanol is used as an intermediate in the synthesis of pharmaceuticals, playing a crucial role in the development of new drugs.
Used in Agricultural Chemicals:
(2-methylphenyl)(diphenyl)methanol is used in the synthesis of agricultural chemicals, helping to develop more effective and safer products for crop protection and other agricultural applications.
Used in Material Development:
(2-methylphenyl)(diphenyl)methanol has potential uses in the development of new materials, owing to its unique chemical structure and properties.
Used as a Research Tool in Chemical Biology:
(2-methylphenyl)(diphenyl)methanol serves as a valuable research tool in chemical biology, aiding scientists in their studies and exploration of biological processes and interactions.
It is important to follow proper safety precautions when handling and using (2-methylphenyl)(diphenyl)methanol to ensure the safety of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 5432-54-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5432-54:
(6*5)+(5*4)+(4*3)+(3*2)+(2*5)+(1*4)=82
82 % 10 = 2
So 5432-54-2 is a valid CAS Registry Number.
5432-54-2Relevant articles and documents
Cinchona alkaloid phase-transfer catalysts revisited: Influence of substituted aryl groups on the enantioselectivity of glycine ester enolate alkylation
Kumar, Sanjeev,Ramachandran, Uma
, p. 7022 - 7028 (2007/10/03)
We report herein, the influence of substituted aryl groups in quaternary ammonium salts derived from cinchona alkaloids on enantioselectivity of the alkylation of glycine ester enolates.
Direct, Low Temperature, in Situ Nucleophilic Aroylation with Aroyllithium Reagents
Seyferth, Dietmar,Hui, Richard C.,Wang, Wei-Liang
, p. 5843 - 5845 (2007/10/02)
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Aroyl Anion Trapping Reactions. A Preliminary Study of Direct Nucleophilic Aroylation by Means of Low Temperature, in situ (CH3)nC6H5 nLi/CO Systems.
Seyferth, Dietmar,Wang, Wei-Liang,Hui, Rihard C.
, p. 1651 - 1654 (2007/10/02)
Results of studies of the in situ nucleophilic aroylation of PhCO2Me, Me3CCO2Me and Ph2CO by several low temperature ArLi/CO systems (Ar = C6H5, p-CH3C6H4, o-CH3C6H4, 2,6-(CH3)2C6H3 and 2,4,6-(CH3)3C6H2) are reported.The experiments with C6H5Li were unsuccessfull and the best results were obtained with 2,6-(CH3)2-C6H3Li.
