33081-37-7 Usage
Description
(βS,2R,5S)-β,5-Dimethyl-5β-vinyltetrahydrofuran-2β-ethanol, also known as vetiverol, is a complex chemical compound derived from the roots of vetiver grass, a plant known for its unique and pleasant aroma. This natural product possesses a woody, earthy, and slightly sweet scent, making it a valuable component in the perfumery and fragrance industry. Beyond its sensory appeal, vetiverol has also garnered interest for its potential pharmacological properties, such as anti-inflammatory and anti-cancer effects, which contribute to its significance in both industrial and medicinal applications.
Uses
Used in Perfumery and Fragrance Industry:
Vetiverol is used as a key ingredient in the perfumery and fragrance industry due to its distinctive woody, earthy, and slightly sweet aroma. Its unique scent adds depth and complexity to various perfumes and fragrance products, enhancing their appeal and making them more attractive to consumers.
Used in Pharmaceutical Research:
Vetiverol is also used as a subject of research in the pharmaceutical industry, particularly for its potential anti-inflammatory and anti-cancer properties. Studies on this compound may lead to the development of new drugs and treatments for various medical conditions, further expanding its applications in the healthcare sector.
Check Digit Verification of cas no
The CAS Registry Mumber 33081-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,8 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33081-37:
(7*3)+(6*3)+(5*0)+(4*8)+(3*1)+(2*3)+(1*7)=87
87 % 10 = 7
So 33081-37-7 is a valid CAS Registry Number.
33081-37-7Relevant articles and documents
INTRAMOLECULAR REACTIONS OF ALLYLOXY RADICALS
Johns, Amanda,Murphy, John A.,Sherburn, Michael S.
, p. 7835 - 7858 (2007/10/02)
Allyloxy radicals formed by epoxide cleavage, have cyclised onto appropriately positioned alkenes to form tetrahydrofurans, and the diastereoselectivity of the cyclisation has been studied.The reaction was used to synthesise lilac alcohols which were then used to confirm the stereochemistry of such cyclisations.
A HIGHLY STEREOSELECTIVE SYNTHESIS OF DAVANONE
Bartlett, Paul A.,Holmes, Christopher P.
, p. 1365 - 1368 (2007/10/02)
Iodocyclization of the anti 4-bromobenzyl ether acetate 4f is a key step in the first stereocontrolled synthesis of the trisubstituted tetrahydrofuran davanone.
