152246-70-3 Usage
Uses
Used in Perfumery and Cosmetics Industry:
Eucamalol is used as a fragrance ingredient in perfumes, soaps, and other scented products for its distinctive camphor-like aroma, enhancing the sensory experience of these products.
Used in Topical Ointments and Skincare Products:
Eucamalol is used as an antimicrobial agent in topical ointments and skincare products to help combat skin infections and promote a healthy skin environment.
Used in Therapeutic Treatments:
Eucamalol is used as a potential therapeutic agent for various medical conditions due to its anti-inflammatory and analgesic effects, making it a promising candidate for the development of treatments for pain relief and inflammation management.
Used in Agricultural and Household Products:
Eucamalol is used as a natural insect repellent in agricultural and household products to protect crops and living spaces from insect infestations, offering an eco-friendly alternative to synthetic insecticides.
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).
