6853-01-6 Usage
Type of compound
Diketone
Structure
Contains a cyclic five-membered ring with a phenyl group attached at the 2nd position
Uses
a. Intermediate in the synthesis of pharmaceuticals
b. Intermediate in the synthesis of dyes
c. Intermediate in the synthesis of other organic compounds
Application in the food industry
Used as a flavoring agent due to its sweet, fruity odor
Application in chemical reactions
Used in the preparation of chiral ligands for asymmetric hydrogenation reactions
Hazardous properties
a. Flammability
b. Irritating effects on the skin
c. Irritating effects on the eyes
Safety precautions
Proper safety measures should be taken when handling this chemical to minimize risks associated with its hazardous properties
Check Digit Verification of cas no
The CAS Registry Mumber 6853-01-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,5 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6853-01:
(6*6)+(5*8)+(4*5)+(3*3)+(2*0)+(1*1)=106
106 % 10 = 6
So 6853-01-6 is a valid CAS Registry Number.
6853-01-6Relevant articles and documents
Forging Fluorine-Containing Quaternary Stereocenters by a Light-Driven Organocatalytic Aldol Desymmetrization Process
Cuadros, Sara,Dell'Amico, Luca,Melchiorre, Paolo
, p. 11875 - 11879 (2017)
Reported herein is a light-triggered organocatalytic strategy for the desymmetrization of achiral 2-fluoro-substituted cyclopentane-1,3-diketones. The chemistry is based on an intermolecular aldol reaction of photochemically generated hydroxy-o-quinodimethanes and simultaneously forges two adjacent fully substituted carbon stereocenters, with one bearing a stereogenic carbon–fluorine unit. The method uses readily available substrates, a simple chiral organocatalyst, and mild reaction conditions to afford an array of highly functionalized chiral 2-fluoro-3-hydroxycyclopentanones.
