53342-22-6 Usage
Chemical class
Esters Compounds formed by the reaction of an acid and an alcohol with the removal of a water molecule.
Formation
Reaction of phenylmethanol with 1-piperidineacetic acid The process by which the ester is formed through an esterification reaction.
Physical state
Colorless liquid The compound appears as a colorless liquid in its pure form.
Odor
Distinct The compound has a noticeable and unique smell.
Applications
Pharmaceutical industry and as a chemical intermediate The compound is used in the production of various pharmaceutical products and serves as a precursor for the synthesis of other compounds.
Safety precautions
Harmful if ingested, inhaled, or comes into contact with the skin The chemical can cause adverse effects if it is swallowed, breathed in, or touches the skin.
Handling and disposal
Follow proper safety protocols It is essential to store and dispose of the chemical according to established safety guidelines to prevent harm to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 53342-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,4 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53342-22:
(7*5)+(6*3)+(5*3)+(4*4)+(3*2)+(2*2)+(1*2)=96
96 % 10 = 6
So 53342-22-6 is a valid CAS Registry Number.
53342-22-6Relevant articles and documents
A de novo peroxidase is also a promiscuous yet stereoselective carbene transferase
Stenner, Richard,Steventon, Jack W.,Seddon, Annela,Anderson, J.L. Ross
, p. 1419 - 1428 (2020/01/28)
By constructing an in vivo-assembled, catalytically proficient peroxidase, C45, we have recently demonstrated the catalytic potential of simple, de novo-designed heme proteins. Here, we show that C45's enzymatic activity extends to the efficient and stereoselective intermolecular transfer of carbenes to olefins, heterocycles, aldehydes, and amines. Not only is this a report of carbene transferase activity in a completely de novo protein, but also of enzyme-catalyzed ring expansion of aromatic heterocycles via carbene transfer by any enzyme.
