338415-92-2 Usage
Uses
Used in Pharmaceutical Industry:
[2-(4-METHOXYPHENYL)CYCLOPROPYL](2-PYRIDINYL)METHANONE is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, [2-(4-METHOXYPHENYL)CYCLOPROPYL](2-PYRIDINYL)METHANONE is used as a building block for the creation of novel agrochemicals, such as pesticides and herbicides. Its structural diversity enables the development of more effective and targeted products.
Used in Material Science:
[2-(4-METHOXYPHENYL)CYCLOPROPYL](2-PYRIDINYL)METHANONE is utilized as a key component in the development of advanced materials with specific properties. Its incorporation into material formulations can lead to improved performance and novel applications in various fields, such as electronics, coatings, and polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 338415-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,8,4,1 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 338415-92:
(8*3)+(7*3)+(6*8)+(5*4)+(4*1)+(3*5)+(2*9)+(1*2)=152
152 % 10 = 2
So 338415-92-2 is a valid CAS Registry Number.
338415-92-2Relevant academic research and scientific papers
Aerobic oxidation of secondary benzylic alcohols and direct oxidative amidation of aryl aldehydes promoted by sodium hydride
Wang, Xinbo,Wang, David Zhigang
supporting information; experimental part, p. 3406 - 3411 (2011/06/17)
We reported herein new reactivities and possible mechanistic implications of a simplest oxidant (NaH/air) uncovered on a broad range of useful transformations, including aerobic alcohol oxidations, allylic alcohol isomerizations and oxidations, cyclopropyl alcohol fragmentations, and direct aryl aldehyde oxidative amidations. These readily implementable transition-metal-free processes feature exceptional material accessibility, operational simplicity, and environmental compatibility, and add new dimensions to its synthetic utilities that are fairly robust yet had not previously been fully realized and systematically explored.
