13567-54-9 Usage
Uses
Used in Perfumery:
(3R,8aβ)-2,3,3a,4,5,6,7,8a-Octahydro-3β,6β,8,8-tetramethyl-1H-3aα,7α-methanoazulene is used as a fragrance ingredient for its woody, musky, and aromatic qualities, adding depth and complexity to perfume compositions.
Used in Traditional Medicine:
In the field of traditional medicine, (3R,8aβ)-2,3,3a,4,5,6,7,8a-Octahydro-3β,6β,8,8-tetramethyl-1H-3aα,7α-methanoazulene is used as a natural remedy for its antimicrobial, anti-inflammatory, and pain-relieving properties, contributing to the treatment of various ailments.
Used in Aromatherapy:
(3R,8aβ)-2,3,3a,4,5,6,7,8a-Octahydro-3β,6β,8,8-tetramethyl-1H-3aα,7α-methanoazulene is used as an essential oil in aromatherapy for its potential to promote relaxation, reduce stress, and provide a soothing atmosphere due to its unique fragrance.
Used in the Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, given its antimicrobial and anti-inflammatory properties, (3R,8aβ)-2,3,3a,4,5,6,7,8a-Octahydro-3β,6β,8,8-tetramethyl-1H-3aα,7α-methanoazulene could potentially be used in the development of new drugs or as an additive in the pharmaceutical industry for treatments involving its known properties.
Check Digit Verification of cas no
The CAS Registry Mumber 13567-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,6 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13567-54:
(7*1)+(6*3)+(5*5)+(4*6)+(3*7)+(2*5)+(1*4)=109
109 % 10 = 9
So 13567-54-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H26/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h10-13H,5-9H2,1-4H3/t10-,11-,12+,13+,15+/m1/s1
13567-54-9Relevant academic research and scientific papers
On the stability and radical deoxygenation of tertiary xanthates
Barton,Parekh,Tse
, p. 2733 - 2736 (2007/10/02)
Xanthates of tertiary alcohols were isolated and properly characterized. Radical deoxygenation reactions under various conditions to the corresponding alkanes were successfully carried out. Comparative data of various initiators and hydrogen atom donors for xanthate deoxygenation are reported.
