155488-34-9 Usage
General Description
1,9-Caryolanediol 9-acetate is a natural organic compound found in various plant species, particularly in essential oils. It is a member of the caryophyllene family and is derived from caryophyllene oxide. The chemical is primarily used in the cosmetic and fragrance industries for its pleasant, woody, and spicy aroma. It is known for its anti-inflammatory and anti-microbial properties, making it a popular ingredient in skincare and personal care products. Additionally, it has shown potential in pharmaceutical applications due to its bioactive properties, indicating potential for use in medicinal products. Overall, 1,9-Caryolanediol 9-acetate is a versatile chemical with various practical applications due to its beneficial properties.
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.
