26532-23-0 Usage
Description
(Z)-3,3-DIMETHYLCYCLOHEXYLIDENEETHANOL is a cyclohexylideneethanol derivative with a (Z) configuration, characterized by its molecular formula C10H20O. This colorless liquid possesses a strong, pungent odor and is insoluble in water, yet soluble in organic solvents. It is a chemical compound known for its low toxicity and safety in specified applications.
Uses
Used in Pharmaceutical and Agrochemical Industries:
(Z)-3,3-DIMETHYLCYCLOHEXYLIDENEETHANOL is utilized as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and agricultural products.
Used in Fragrance Industry:
In the personal care and household products sector, (Z)-3,3-DIMETHYLCYCLOHEXYLIDENEETHANOL serves as a fragrance ingredient, enhancing the scent profiles of different consumer goods.
Used as a Chemical Intermediate:
(Z)-3,3-DIMETHYLCYCLOHEXYLIDENEETHANOL also has potential applications as a chemical intermediate in the production of other organic compounds, expanding its utility across various chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 26532-23-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,3 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 26532-23:
(7*2)+(6*6)+(5*5)+(4*3)+(3*2)+(2*2)+(1*3)=100
100 % 10 = 0
So 26532-23-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-8(11)9-5-4-6-10(2,3)7-9/h11H,4-7H2,1-3H3/b9-8-
26532-23-0Relevant articles and documents
THE STEREOSPECIFIC FORMATION OF AN EXOCYCLIC ALKENE BY A CONSECUTIVE RADICAL CYCLIZATION-ELEIMINATION
Harris, Francis L.,Weiler, Larry
, p. 2941 - 2944 (1987)
The iodovinylstannanes 4 and 5 were prepared by the conjugate addition of the tri-n-butyltin moiety to a substituted propiolic ester.Compounds 4 and 5 underwent a radical cyclization-elimination reaction to stereospecifically generate an exocyclic alkene.
SYNTHETIC STUDIES ON THE OCHTODANE TYPE TERPENES I. STEREOSELECTIVE CONSTRUCTION OF THE OCHTODANE SKELETON FROM MYRCENE.
Masaki,Hashimoto,Sakuma,Kaji
, p. 3466 - 3475 (2007/10/02)
The ochtodane skeleton, the Carbon framework of 1,1-dimethyl-3-ethylcyclohexane (1) was constructed highly stereoselectively by the acid-catalyzed (SnCl//4 or CF//3CO//2H) cyclization of the terminally functionalized myrcene derivatives, the benzenesulfenyl chloride adduct (7), the terminal beta -hydroxy sulfide (8) derived from 7, and myrcene 6,7-epoxide (10). The stereoselectivity of the 3-exo-double bond in 1 formed concomitantly in the cyclization reaction was found to depend remarkably upon the reaction temperture and the 85-94% of E-stereoselectivity was attained at minus 78 degree C. By the method, the ochtodane derivatives with the sulfur- or oxygen-functional groups on the C(6)-position were obtained.
