4017-92-9 Usage
Uses
Used in Pharmaceutical Industry:
(+)-Caran-3beta-ol is used as an active pharmaceutical ingredient for its anti-inflammatory and analgesic properties, helping to alleviate pain and reduce inflammation in various conditions.
Used in Fragrance Industry:
(+)-Caran-3beta-ol is used as a fragrance ingredient for its distinct sweet, woody, and pine-like odor, contributing to the creation of various scent profiles in perfumes, cosmetics, and other scented products.
Used in Pest Control Industry:
(+)-Caran-3beta-ol is used as an insect repellent and insecticide due to its ability to repel insects, making it a potential component in the development of pest control products.
Used in Anticancer Research:
(+)-Caran-3beta-ol is used as a novel anticancer agent in research studies, exploring its potential to target and inhibit the growth of cancer cells.
Used in Insect Repellent Products:
(+)-Caran-3beta-ol is used as an active ingredient in insect repellent products to provide protection against insect bites and reduce the risk of insect-borne diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 4017-92-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,1 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4017-92:
(6*4)+(5*0)+(4*1)+(3*7)+(2*9)+(1*2)=69
69 % 10 = 9
So 4017-92-9 is a valid CAS Registry Number.
4017-92-9Relevant academic research and scientific papers
LIGHT-MEDIATED TRANSFORMATIONS OF OLEFINS INTO ALCOHOLS: REACTIONS OF HYDROXYL RADICALS WITH CYCLOALKENES
Sonawane, H. R.,Nanjundiah, B. S.,Kelkar, R. G.
, p. 6673 - 6682 (2007/10/02)
Reactions of hydroxyl radicals, generated by photodecomposition of hydrogen peroxide in acetonitrile, with a wide variety of cycloalkenes have been examined.The results show that the major reaction is the addition of hydroxyl radicals to the less substituted end of the double bond, furnishing the secondary alcohols.The reactivity pattern and the observed regio- and stereoselectivity clearly reveal that the steric parameters associated with the substrates play a dominant role in directing the addition reactions.More importantly, this study led to the development of a new methodology for the facile conversions of olefins essentially into secondary alcohols, and includes a few examples which demonstrate the potential of the method.
REARRANGEMENTS OF MONOTERPENES IN FUSED ORGANIC ACID
Angelis, Francesco De,Ferretti, Gabriella,Botta, Maurizio,Nicoletti, Rosario
, p. 499 - 500 (2007/10/02)
Rearrangements of terpenic alcohols are significantly influenced by the nature of the organic acid used as the reaction medium.The formation of neoisothujyl alcohol is a highly favoured process in abietic acid.
