7399-56-6 Usage
Description
1-(1-ethylcyclohexyl)-4-methylbenzene, also known as 1-isopropyl-4-methylcyclohexane or p-Isopropyl-p-xylene, is a chemical compound with the molecular formula C15H24. It is a colorless liquid that has a distinct odor and is recognized for its versatile applications in various industries.
Uses
Used in the Chemical Industry:
1-(1-ethylcyclohexyl)-4-methylbenzene is used as a solvent for various applications due to its chemical properties. It aids in the manufacturing process of different products by dissolving and mixing with other substances, facilitating chemical reactions.
Used in the Dye and Perfume Industry:
1-(1-ethylcyclohexyl)-4-methylbenzene is utilized in the production of dyes and perfumes, where it serves as a key ingredient. Its distinct odor and chemical composition make it suitable for creating a wide range of scents and colors.
Used in Cosmetic and Personal Care Products:
1-(1-ethylcyclohexyl)-4-methylbenzene is also used as a fragrance ingredient in the cosmetic and personal care industry. Its distinct scent adds value to various products, enhancing their appeal to consumers.
Safety Note:
It is crucial to handle 1-(1-ethylcyclohexyl)-4-methylbenzene with care, as it can be hazardous if not used properly. Proper safety measures should be taken to minimize any potential risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 7399-56-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7399-56:
(6*7)+(5*3)+(4*9)+(3*9)+(2*5)+(1*6)=136
136 % 10 = 6
So 7399-56-6 is a valid CAS Registry Number.
7399-56-6Relevant articles and documents
SYNTHESIS OF p-(1-ALKYLCYCLOHEXYL)BENZOIC ACIDS
Obukhova, T. A.,Basaeva, N. N.,Betnev, A. F.,Musabekov, Yu. Yu.,Mironov, G. S.
, p. 351 - 353 (2007/10/02)
A series of new p-(1-alkylcyclohexyl)benzoic acids were obtained by the alkylation of toluene with 4-alkylcyclohexanols followed by oxidation of the alkylation products.
