2808-12-0 Usage
Description
(Cyclohexyl-3) acetate de methyle, also known as methyl cyclohexyl-3 acetate, is a chemical compound with the molecular formula C9H16O2. It is a colorless liquid characterized by a fruity, floral odor. This versatile chemical is synthesized through the esterification of cyclohexanone with methanol, making it a valuable ingredient across different industries due to its distinct sensory properties.
Uses
Used in Fragrance Industry:
(Cyclohexyl-3) acetate de methyle is used as a fragrance ingredient for its fruity, floral scent, adding a pleasant aroma to perfumes and personal care products. Its ability to provide a fresh and appealing scent makes it a popular choice in the fragrance industry.
Used in Flavor and Food Industry:
In the flavor and food industry, (cyclohexyl-3) acetate de methyle is used as a flavoring agent. Its unique fruity and floral notes enhance the taste and aroma of various food and beverage products, contributing to a more enjoyable consumer experience.
These applications highlight the diverse utility of (cyclohexyl-3) acetate de methyle in different sectors, primarily driven by its distinctive sensory characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 2808-12-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2808-12:
(6*2)+(5*8)+(4*0)+(3*8)+(2*1)+(1*2)=80
80 % 10 = 0
So 2808-12-0 is a valid CAS Registry Number.
2808-12-0Relevant articles and documents
Rhodium-Catalyzed Annelation of Benzoic Acids with α,β-Unsaturated Ketones with Cleavage of C?H, CO?OH, and C?C Bonds
Zhang, Guodong,Hu, Zhiyong,Belitz, Florian,Ou, Yang,Pirkl, Nico,Goo?en, Lukas J.
, p. 6435 - 6439 (2019/04/10)
In the presence of a [Cp*RhCl2]2 catalyst, the Lewis acid In(OTf)3, and the mild base Na2CO3, aromatic carboxylates and α,β-unsaturated ketones undergo a unique hydroarylation/Claisen/retro-Claisen pr
An environmentally friendly procedure for Mukaiyama aldol and Mukaiyama-Michael reactions using a catalytic amount of DBU under solvent- and metal-free conditions
Shen, Zhi-Liang,Ji, Shun-Jun,Loh, Teck-Peng
, p. 507 - 508 (2007/10/03)
Mukaiyama aldol and Mukaiyama-Michael reactions can proceed smoothly in the presence of a catalytic amount of DBU (20% mmol), to afford the corresponding products in moderate to good yields. This solvent- and metal-free approach provides an environmentall
Highly regioselective addition of an ester enolate equivalent to α,β-unsaturated ketones: Selective formation of both isomers derived from 1,2- and 1,4-additions using α-stannyl ester with additives
Yasuda,Matsukawa,Okamoto,Sako,Kitahara,Baba
, p. 2149 - 2150 (2007/10/03)
The reaction of α-stannyl ester with α,β-unsaturated ketones in the presence of stannous chloride (SnCl2) and chlorosilanes (Me3SiCl or Me2SiCl2) gave 1,2- and 1,4-addition products, respectively.
