19096-86-7 Usage
General Description
(1Z)-5-methyl-2-(1-methylethyl)cyclohexanone oxime, also known as menthone oxime, is a chemical compound with the molecular formula C10H19NO. It is an oxime derivative of menthone, which is a naturally occurring compound found in peppermint oil. Menthone oxime has a unique molecular structure, with a cyclohexanone ring and an oxime functional group attached to it. It is commonly used in the synthesis of various organic compounds, as well as in the production of fragrances and flavors. Menthone oxime has a minty, camphor-like odor and is known for its cooling sensation when applied to the skin, making it a popular ingredient in topical analgesic products. It is also used as a flavor and fragrance additive in the food and beverage industry. Additionally, menthone oxime has been studied for its potential biological and pharmacological activities, including antioxidant and antimicrobial properties.
Check Digit Verification of cas no
The CAS Registry Mumber 19096-86-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,9 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19096-86:
(7*1)+(6*9)+(5*0)+(4*9)+(3*6)+(2*8)+(1*6)=137
137 % 10 = 7
So 19096-86-7 is a valid CAS Registry Number.
19096-86-7Relevant articles and documents
Tandem and Selective Conversion of Tetrahydropyranyl and Silyl Ethers to Oximes Catalyzed with Trichloroisocyanuric Acid
Aghapour, Ghasem,Abbaszadeh, Zeinab
, p. 1464 - 1470 (2015/09/01)
Direct and oxidative conversion of tetrahydropyranyl and silyl ethers to oximes is described using trichloroisocyanuric acid (TCCA) as a relatively stable and inexpensive oxidant surprisingly in a catalytic amount and hydroxylamine hydrochloride under solvent-free conditions. Oximes can be synthesized from these protected alcohols in the presence of some other functional groups with excellent chemoselectivity using the present tandem catalytic method.
LIQUID CHROMATOGRAPHIC RESOLUTION OF RACEMIC KETONES AS THEIR OXIME 3,5-DINITROPHENYL CARBAMATES ON A CHIRAL STATIONARY PHASE
Hyun, Myung Ho,Park, Young -Whan,Baik, In-Kyu
, p. 4735 - 4738 (2007/10/02)
Cyclic and acyclic chiral ketones have been resolved as their oxime 3,5-dinitrophenyl carbamates on a chiral stationary phase derived from (S)-1-(6,7-dimethyl-1-naphthyl)isobutylamine.
