152246-70-3 Usage
General Description
Eucamalol is a chemical compound found in various essential oils, including eucalyptus and camphor oil. It is characterized by its distinctive camphor-like aroma and is commonly used in the production of perfumes, soaps, and other scented products. Eucamalol has been found to possess antimicrobial properties and is often used as an ingredient in topical ointments and skincare products. Additionally, it has been studied for its potential anti-inflammatory and analgesic effects, making it a promising candidate for the development of therapeutic treatments for various medical conditions. Eucamalol is also known to have insecticidal properties and is often used as a natural insect repellent in agricultural and household products.
Check Digit Verification of cas no
The CAS Registry Mumber 152246-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,2,4 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 152246-70:
(8*1)+(7*5)+(6*2)+(5*2)+(4*4)+(3*6)+(2*7)+(1*0)=113
113 % 10 = 3
So 152246-70-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O2/c1-7(2)9-4-3-8(6-11)5-10(9)12/h5-7,9-10,12H,3-4H2,1-2H3/t9-,10-/m0/s1
152246-70-3Relevant articles and documents
Absolute configuration of a new mosquito repellent, (+)-eucamalol and the repellent activity of its epimer.
Satoh,Utamura,Nakade,Nishimura
, p. 1139 - 1141 (2007/10/02)
(+)-Eucamalol (1) and (-)-1-epi-eucamalol (2) were synthesized from (S)-(-)-perillaldehyde to determine the absolute configuration of 1, the structure of natural (+)-eucamalol being determined to be (1R,6R)-(+)-3-formyl-6-isopropyl-2-cyclohexen-1-ol. (+)-
Novel Rearrangement of 2α-Isopropyl-8-oxabicyclooct-6-ene Producing the Monoterpene 3-Hydroxyphellandral
Barbosa, Luiz Claudio de Almeido,Demuner, Antonio J.,Mann, John,Veloso, Dorila P.
, p. 585 - 588 (2007/10/02)
We describe a five-step synthesis of 2α-isopropyl-8-oxabicyclooct-6-ene from 1,1,3,3-tetrabromo-4-methylpentan-2-one, and its unexpected rearrangement to yield trans-3-hydroxy-4-isopropylcyclohex-1-enecarbaldehyde (3-hydroxyphellandral).
