4586-97-4 Usage
Description
(3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-Tetramethyl-18-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3,5,7,9,11,13,15,17-octadecaocten-2-one is a long-chain, highly unsaturated ketone with 18 carbon atoms and eight evenly spaced double bonds. Its numerous double bonds make it highly reactive and prone to oxidation, while its lipophilic nature allows for use in various applications.
Uses
Used in Cosmetics and Personal Care Products:
(3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-Tetramethyl-18-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3,5,7,9,11,13,15,17-octadecaocten-2-one is used as a fragrance ingredient in the formulation of cosmetics and personal care products due to its highly reactive and lipophilic properties.
Used in Organic Synthesis:
(3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-Tetramethyl-18-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3,5,7,9,11,13,15,17-octadecaocten-2-one has potential applications in the field of organic synthesis for the preparation of various compounds, taking advantage of its complex structure and reactivity.
Used in Fragrance Industry:
(3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-Tetramethyl-18-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3,5,7,9,11,13,15,17-octadecaocten-2-one is used as a fragrance ingredient in the fragrance industry, where its unique scent profile can be utilized in creating various scent compositions.
Check Digit Verification of cas no
The CAS Registry Mumber 4586-97-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,8 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4586-97:
(6*4)+(5*5)+(4*8)+(3*6)+(2*9)+(1*7)=124
124 % 10 = 4
So 4586-97-4 is a valid CAS Registry Number.
4586-97-4Relevant articles and documents
Total Synthesis of C31-Methyl Ketone Apocarotenoids: Sintaxanthin and (3R)-3-Hydroxysintaxanthin
Haugan, Jarle Andre
, p. 657 - 664 (2007/10/02)
The previously undescribed (all-E)-2,7,11-trimethyl-12-oxo-2,4,6,8,10-tridecapentenal has been synthesised in 26percent overall yield in six steps from the readily available 3-methyl-2-penten-4-yn-1-ol and 2,7-dimethyl-2,4,6-octatrienedial.This C16-keto aldehyde was used in the first total synthesis of fully characterised (all-E)-sintaxanthin and optically active (all-E)-(3R)-3-hydroxysintaxanthin.The C16-keto aldehyde is a versatile building block for any C31-methyl ketone apocarotenoid.
