236117-38-7 Usage
General Description
1-Propanone, 2-iodo-1-(4-methylphenyl)- is a chemical compound with the molecular formula C10H11IO. It is also known by its systematic name 2-iodo-1-(4-methylphenyl)propan-1-one. 1-Propanone, 2-iodo-1-(4-methylphenyl)- is a derivative of propanone (acetone) with an iodine atom and a methylphenyl group attached to the carbon chain. It is commonly used in organic synthesis and pharmaceutical research as a reagent or intermediate. The presence of the iodine atom and the aromatic methylphenyl group gives this compound unique chemical properties, making it useful in various chemical reactions and applications. Due to its specific structure and properties, 1-Propanone, 2-iodo-1-(4-methylphenyl)- has potential uses in the development of new drugs and other fine chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 236117-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,6,1,1 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 236117-38:
(8*2)+(7*3)+(6*6)+(5*1)+(4*1)+(3*7)+(2*3)+(1*8)=117
117 % 10 = 7
So 236117-38-7 is a valid CAS Registry Number.
236117-38-7Relevant articles and documents
α,α-Alkylation-Halogenation and Dihalogenation of Sulfoxonium Ylides. A Direct Preparation of Geminal Difunctionalized Ketones
Gallo, Rafael D. C.,Ahmad, Anees,Metzker, Gustavo,Burtoloso, Antonio C. B.
, p. 16980 - 16984 (2017/11/27)
A one-pot alkylation–halogenation of ketosulfoxonium ylides in the presence of alkyl halides is described. The method furnishes several gem-difunctionalized haloketones (an alkyl and F, Cl, Br, or I) in good yields. Replacing alkyl halides with a mixture of electrophilic halogen species and various halide anions led to gem-dihalogenated ketones containing a combination of the same or two different halogens. Kinetic isotopic effects as well as reaction kinetic experiments give insight to the mechanism of these reactions.
Efficient α-iodination of carbonyl compounds under solvent-free conditions using microwave irradiation
Lee, Jong Chan,Bae, Yong Hun
, p. 507 - 508 (2007/10/03)
Direct conversion of carbonyl compounds into α-iodocarbonyl compounds has been successfully achieved under solvent-free microwave irradiation conditions using N-iodosuccinimide and p-toluenesulfonic acid.
