5457-86-3 Usage
Chemical compound
A substance formed by a chemical reaction with a specific molecular structure.
Complex molecular structure
The compound has a complex arrangement of atoms and bonds.
Derivative of phenylacetate
It is derived from the parent compound phenylacetate.
Phenylacetate
A compound commonly used in organic synthesis and pharmaceutical research.
1,3-benzodioxol-5-ylmethyl group
A distinct aromatic and potentially bioactive component attached to the phenylacetate molecule.
Aromatic component
The compound has an aromatic ring structure, which contributes to its unique properties.
Potential bioactivity
The compound may have biological activity, which could be useful in pharmaceutical research.
Applications
It may have potential applications in the development of new pharmaceuticals, fragrances, or other industrial products.
Further research needed
More research is required to fully understand the properties and potential uses of the compound.
Check Digit Verification of cas no
The CAS Registry Mumber 5457-86-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5457-86:
(6*5)+(5*4)+(4*5)+(3*7)+(2*8)+(1*6)=113
113 % 10 = 3
So 5457-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O4/c17-16(9-12-4-2-1-3-5-12)18-10-13-6-7-14-15(8-13)20-11-19-14/h1-8H,9-11H2
5457-86-3Relevant academic research and scientific papers
Palladium-catalyzed carbonylation of benzylic ammonium salts to amides and esters: Via C-N bond activation
Yu, Weijie,Yang, Shuwu,Xiong, Fei,Fan, Tianxiang,Feng, Yan,Huang, Yuanyuan,Fu, Junkai,Wang, Tao
supporting information, p. 3099 - 3103 (2018/05/22)
An efficient palladium-catalyzed carbonylation reaction of readily available quaternary ammonium salts with CO is reported for the first time to afford arylacetamides and arylacetic acid esters via benzylic C-N bond cleavage. This protocol features mild reaction conditions under atmospheric pressure of CO, a redox-neutral process without an additional oxidant, and a broad substrate scope for various kinds of amines, alcohols and phenols.
