30960-39-5 Usage
Description
[3R-(3alpha,3abeta,7beta,8aalpha)]-1,2,3,7,8,8a-hexahydro-3,6,8,8-tetramethyl-4H-3a,7-methanoazulen-4-one is a bicyclic sesquiterpene ketone with a complex molecular structure, featuring a fused-ring system and functional groups such as carbonyl and methyl groups. This chemical compound is commonly found in various natural sources, including certain plants and essential oils, where it plays significant biological and physiological roles.
Uses
Used in Fragrance Industry:
[3R-(3alpha,3abeta,7beta,8aalpha)]-1,2,3,7,8,8a-hexahydro-3,6,8,8-tetramethyl-4H-3a,7-methanoazulen-4-one is used as a key compound in the fragrance industry for its unique scent properties, contributing to the creation of various fragrances and perfumes.
Used in Flavor Industry:
In the flavor industry, [3R-(3alpha,3abeta,7beta,8aalpha)]-1,2,3,7,8,8a-hexahydro-3,6,8,8-tetramethyl-4H-3a,7-methanoazulen-4-one is utilized as an essential component in the development of distinct flavors for the food and beverage sector, enhancing the taste and aroma of various products.
Used in Pharmaceutical Industry:
[3R-(3alpha,3abeta,7beta,8aalpha)]-1,2,3,7,8,8a-hexahydro-3,6,8,8-tetramethyl-4H-3a,7-methanoazulen-4-one is used as a building block in the pharmaceutical industry for synthesizing other compounds and products, thanks to its unique structure and properties, which can be harnessed for the development of new drugs and medications.
Check Digit Verification of cas no
The CAS Registry Mumber 30960-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,9,6 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 30960-39:
(7*3)+(6*0)+(5*9)+(4*6)+(3*0)+(2*3)+(1*9)=105
105 % 10 = 5
So 30960-39-5 is a valid CAS Registry Number.
30960-39-5Relevant articles and documents
Cedar camphor derivative as well as preparation method and application thereof
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, (2021/04/03)
The invention relates to the technical field of synthetic drugs, in particular to a cedar camphor derivative as well as a preparation method and an application thereof. The cedar camphor derivative isany one of compounds shown in the following structural formula, tautomers, hydrates, solvates or pharmaceutically acceptable salts thereof, and the cedar camphor derivative has a good treatment effect on viruses, especially influenza viruses, so that the application range of the cedar camphor and the derivatives thereof is expanded, and the variety of the cedar camphor derivatives is expanded.
Functionalisation of Saturated Hydrocarbons. Part IX. Oxidation of Cedrol, β- and γ-Eudesmol, Sclareol, Manoyl Oxide, 1,9-Dideoxyforskolin, Methyl trans-Dihydrojasmonate, and Tetrahydrolinalool by the 'Gif System'
Barton, Derek H. R.,Beloeil, Jean-Claude,Billion, Annick,Boivin, Jean,Lallemand, Jean-Yves,et al.
, p. 2187 - 2200 (2007/10/02)
The oxidation of cedrol (1), β- and γ-eudesmol (6 and 7, resp.), sclareol (14), manoyl oxide (15), 1,9-dideoxyforskolin (22) (+/-)-methyl trans-dihydrojasmonate (28), and tetrahydrolinalool (32), nearly all of natural terpenoid origin, by the 'Gif system' has afforded a number of novel products (3, 11, and 12, 16/17, 18/19, 26, 29-31, and ketones corresponding to 34-35, resp.).The structures of these compounds were established by spectroscopic techniques including 2D-NMR and, where appropriate, by comparison with authentic samples.
