3242-05-5 Usage
Description
(1S,4aβ)-Decahydro-1β,8aβ-dimethyl-7β-(1-methylethyl)naphthalene, commonly known as longifolene, is a bicyclic hydrocarbon with a complex molecular structure consisting of ten carbon atoms arranged in a ring. It features two methyl groups and one isopropyl group attached, giving it a distinct chemical profile. This organic compound is found in various natural sources, such as essential oils from pine trees and other coniferous plants, known for its pleasant, pine-like odor.
Uses
Used in Fragrance and Flavoring Industries:
(1S,4aβ)-Decahydro-1β,8aβ-dimethyl-7β-(1-methylethyl)naphthalene, or longifolene, is utilized as a key ingredient in the fragrance and flavoring industries due to its characteristic pine-like aroma. Its natural and appealing scent makes it a popular choice for creating perfumes, colognes, and other scented products, as well as for enhancing the flavor profiles of various food and beverage items.
Used in Adhesives and Coatings Production:
Longifolene also finds applications in the manufacturing of adhesives, coatings, and other industrial products. Its unique chemical properties contribute to the development of high-quality and durable products that are used across different sectors, including construction, automotive, and manufacturing industries. (1S,4aβ)-Decahydro-1β,8aβ-dimethyl-7β-(1-methylethyl)naphthalene's versatility and stability make it a valuable component in these applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3242-05-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,4 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3242-05:
(6*3)+(5*2)+(4*4)+(3*2)+(2*0)+(1*5)=55
55 % 10 = 5
So 3242-05-5 is a valid CAS Registry Number.
3242-05-5Relevant articles and documents
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Ishii,H. et al.
, p. 1545 - 1548 (1966)
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(-)-1(10),11-Eremophiladien-9β-ol from the liverwort Marchantia polymorpha ssp. aquatica
Rieck, Angela,Buelow, Nils,Fricke, Christiane,Saritas, Yuecel,Koenig, Wilfried A.
, p. 195 - 197 (2007/10/03)
A new eremophilane-type sesquiterpenoid, (-)-1(10),11-eremophiladien- 9β-ol, was isolated from the liverwort Marchantia polymorpha ssp. aquatica. Structure elucidation was performed by means of spectroscopic methods and chemical conversion to known eremophilone. The configuration was proved by NOE measurements and comparison of the products obtained by dehydration and hydrogenation of the alcohol with the hydrogenation products of both enantiomers of eremophilene and valencene by enantioselective gas chromatography with cyclodextrin derivatives.
STEREOSPECIFIC TOTAL SYNTHESES OF 7α- AND 7β-EREMOPHILANE-6-ONE AND 7α- AND 7β-EREMOPHILANE
Jacobi, Peter A.,Frechette, Roger F.
, p. 2937 - 2940 (2007/10/02)
The title compounds have been prepared in a highly efficient fashion by a synthetic route involving an intramolecular Diels-Alder reaction of an acetylenic thiazole followed by reductive modification of the resulting fused-ring thiophene.
