7463-83-4 Usage
Uses
Used in Fragrance Industry:
Phenyl(pyridin-2-yl)methyl benzoate is utilized as a fragrant ingredient in perfumes and cosmetics, capitalizing on its pleasant odor to enhance the sensory experience of these products.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, phenyl(pyridin-2-yl)methyl benzoate serves as a key intermediate in the synthesis of various drugs, contributing to the development of new medicinal compounds.
Used in Agrochemical Synthesis:
Similarly, in agrochemicals, phenyl(pyridin-2-yl)methyl benzoate is employed in the synthesis of different agrochemical products, playing a role in the creation of substances that protect and enhance crop yields.
Used in Organic Chemistry Research:
Phenyl(pyridin-2-yl)methyl benzoate is also valuable in organic chemistry research, where it can be used to explore new reactions, mechanisms, and the synthesis of complex organic molecules. Its stable and non-reactive nature allows for predictable and controlled experimentation.
Check Digit Verification of cas no
The CAS Registry Mumber 7463-83-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7463-83:
(6*7)+(5*4)+(4*6)+(3*3)+(2*8)+(1*3)=114
114 % 10 = 4
So 7463-83-4 is a valid CAS Registry Number.
7463-83-4Relevant academic research and scientific papers
Acylation of 2-benzylpyridine N-oxides and subsequent in situ [3,3]-sigamatropic rearrangement reaction
Antilla, Jon C.,Jing, Hua-qing,Li, Hong-liang
, (2020/09/22)
An effective method for the acylation of 2-benzylpyridine N-oxides and their fast in situ [3,3]-sigmatropic rearrangement was reported. This transformation has a wide substrate scope under mild conditions, giving moderate to excellent yields. The application for the synthesis of chiral phenyl-2-pyridylmethanol products was briefly explored. Furthermore, an interesting example of tandem substitution and in situ [3,3]-sigamatropic rearrangement of 2-benzylpyridine N-oxide with benzenecarboximidoyl chloride was reported.
