13828-31-4 Usage
Physical state
Colorless liquid
This compound appears as a colorless liquid under normal conditions.
Usage in manufacturing
Perfumes and pharmaceuticals
1-Methyl-3-(1-methylethyl)cyclohexene is used as a key ingredient in the production of various perfumes and pharmaceutical products.
Chemical classification
Cyclic hydrocarbon (Cycloalkene)
This compound is a type of cyclic hydrocarbon, specifically a cycloalkene, which means it contains a cyclohexene ring structure.
Substituents
Methyl and isopropyl groups
In its structure, 1-Methyl-3-(1-methylethyl)cyclohexene has a methyl group and an isopropyl group attached to the cyclohexene ring.
Application as flavoring agent
Food products
Due to its unique properties, 1-Methyl-3-(1-methylethyl)cyclohexene is used as a flavoring agent in various food products.
Check Digit Verification of cas no
The CAS Registry Mumber 13828-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,2 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13828-31:
(7*1)+(6*3)+(5*8)+(4*2)+(3*8)+(2*3)+(1*1)=104
104 % 10 = 4
So 13828-31-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H18/c1-8(2)10-6-4-5-9(3)7-10/h7-8,10H,4-6H2,1-3H3
13828-31-4Relevant articles and documents
Cu(I)-catalyzed, α-selective, allylic alkylation reactions between phosphorothioate esters and organomagnesium reagents
Lauer, Andrew M.,Mahmud, Farzeen,Wu, Jimmy
supporting information; experimental part, p. 9119 - 9123 (2011/08/04)
Regiocontrol of allylic alkylation reactions involving hard nucleophiles remains a significant challenge and continues to be an active area of research. The lack of general methods in which α-alkylation is favored underscores the need for the development of new processes for achieving this type of selectivity. We report that Cu(I) catalyzes the allylic substitution of phosphorothioate esters with excellent α-regioselectivity, regardless of the nature of the Grignard reagent that is used. To the best of our knowledge, the Cu-catalyzed allylic alkylation of phosphorothioate esters has never been described. We have also developed a simple protocol for inducing high α selectivity starting from secondary allylic halides. This is accomplished by using sodium phosphorothioates as an additive.
