52475-86-2 Usage
General Description
1-methyl-4-(4-methyl-3-pentenyl)cyclohex-3-ene-1-carbaldehyde is a chemical compound with a complex molecular structure. It is a cyclic compound containing a cyclohexene ring with a carbaldehyde group attached to it. The molecule also contains a side chain consisting of a methyl group and a 4-methyl-3-pentenyl group. 1-methyl-4-(4-methyl-3-pentenyl)cyclohex-3-ene-1-carbaldehyde is commonly used in the production of perfumes and fragrances, as it contributes to their unique and pleasant scent. It is also used in the manufacture of flavoring agents and other aromatic products. Additionally, it has been found to exhibit antimicrobial properties and is being researched for potential pharmaceutical applications. Due to its complex structure and aromatic properties, 1-methyl-4-(4-methyl-3-pentenyl)cyclohex-3-ene-1-carbaldehyde is a versatile compound with diverse industrial and scientific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 52475-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,7 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52475-86:
(7*5)+(6*2)+(5*4)+(4*7)+(3*5)+(2*8)+(1*6)=132
132 % 10 = 2
So 52475-86-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H22O/c1-12(2)5-4-6-13-7-9-14(3,11-15)10-8-13/h5,7,11H,4,6,8-10H2,1-3H3
52475-86-2Relevant articles and documents
The search for new odorants: Synthesis of animalic fragrant and musky/ambery compounds
Plessis, Caroline
, p. 1517 - 1539 (2015/03/03)
An overview of the recent research which allowed us to discover novel animalic odorants is presented. The new derivatives were prepared from readily available starting materials via easy reaction steps in good yields. They possess very different structures, such as bicyclic pentanols, glycolates, or tricyclic ketones, and all show interesting notes in the animalic fragrant family: from costus, leathery to ambery and musky scents, making them all attractive for different purposes.
Cycloaddition Of Carbonyl Compounds To Olefins At Aluminosilicate Catalysts
Volcho, K. P.,Tatarova, L. E.,Korchagina, D. V.,Salakhutdinov, N. F.,Aul'chenko, I. S.,et al.
, p. 683 - 694 (2007/10/02)
The use of zeolite catalysts in the reactions of allocimene and myrcene with α,β-unsaturated carbonyl compounds makes the reaction conditions milder and increases both the regio- and the stereoselectivity of the diene synthesis processes.In the reaction of certain polyenes with aldehydes at ascanite-bentonite clay a new reaction, leading to bicyclic ethers, was discovered.
