39863-86-0 Usage
Structure
An ethyl ester derivative of 2,4-pentadienoic acid with a 3-methyl-5-(2,6,6-trimethyl-2-cyclohexen-1-yl) group
Isomer
(E,E) isomer
Physical properties
Colorless liquid with a fruity, floral, and slightly balsamic odor
Uses
Commonly used in the fragrance and flavoring industry, as well as in the production of cosmetics and as an intermediate in the synthesis of other organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 39863-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,6 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39863-86:
(7*3)+(6*9)+(5*8)+(4*6)+(3*3)+(2*8)+(1*6)=170
170 % 10 = 0
So 39863-86-0 is a valid CAS Registry Number.
39863-86-0Relevant academic research and scientific papers
BIOSYTESIS OF ABSCISIC ACID FROM &α-IONYLIDENEETHANOL IN CERCOSPORA PINI-DENSIFLORAE
Okamoto, Masahiko,Hirai, Nobuhiro,Koshimizu, Koichi
, p. 3465 - 3470 (2007/10/02)
2H-labelled α-ionylideneethanol was efficiently incorporated into the 1',4'-trans-diol of ABA via (1'R)-4'S-hydroxy-α-ionylideneacetic acid by Cercospora pini-densiflorae, and 2H-labelled α-ionylideneacetic acid was incorporated into 1'-deoxyABA via (1'R)
Further Synthesis of Zeaxanthin and Rhodoxanthin
Ellis, Peter R.,Faruk, Erol A.,Moss, Gerald P.,Weedon, Basil C. L.
, p. 1092 - 1097 (2007/10/02)
A modification of a previously reported synthesis of zeaxanthin (1), and routes to both zeaxanthin and rhodoxanthin (2) from α-ionone, are described.
