155488-34-9 Usage
Description
1,9-Caryolanediol 9-acetate is a natural organic compound belonging to the caryophyllene family, derived from caryophyllene oxide and found in various plant species, particularly in essential oils. It is characterized by its pleasant, woody, and spicy aroma, along with its anti-inflammatory and anti-microbial properties, making it a valuable ingredient in various industries.
Uses
Used in Cosmetic and Fragrance Industry:
1,9-Caryolanediol 9-acetate is used as a fragrance ingredient for its pleasant, woody, and spicy aroma, adding depth and complexity to perfumes and other scented products.
Used in Skincare and Personal Care Products:
1,9-Caryolanediol 9-acetate is used as an active ingredient in skincare and personal care products for its anti-inflammatory and anti-microbial properties, contributing to the health and well-being of the skin.
Used in Pharmaceutical Applications:
1,9-Caryolanediol 9-acetate is used as a potential medicinal ingredient due to its bioactive properties, indicating its potential for use in the development of new pharmaceutical products.
Check Digit Verification of cas no
The CAS Registry Mumber 155488-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,4,8 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 155488-34:
(8*1)+(7*5)+(6*5)+(5*4)+(4*8)+(3*8)+(2*3)+(1*4)=159
159 % 10 = 9
So 155488-34-9 is a valid CAS Registry Number.
155488-34-9Relevant articles and documents
Constituents of Sindora sumatrana MIQ. I. Isolation and NMR spectral analysis of sesquiterpenes from the dried pods
Heymann,Tezuka,Kikuchi,Supriyatna
, p. 138 - 146 (2007/10/02)
Investigation of the neutral fraction of the dried pods of Sindora sumatrana MIQ. has resulted in the isolation of three new sesquiterpenoids (2, 6 and 8) together with nine known ones (1, 3, 4, 5, 7, 9, 10, 11a and 12a), of which three (7, 10 and 12a) are reported for the first time from a natural source. One other compound, 4-stigmasten-3-one (13) (together with a sterol mixture; β-sitosterol, stigmasterol and campesterol) was also obtained. The structures of all the isolated sesquiterpenes were determined by means of spectroscopic methods, mainly two-dimensional NMR techniques, and the compounds were found to have the caryophyllane, humulane, clovane and caryolane skeletons. The NMR data of the isolated sesquiterpenes are also discussed.
