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N-methyl-2-phenylbutanamide is a chemical compound with the molecular formula C12H17NO. It is a white crystalline solid that is soluble in organic solvents. N-methyl-2-phenylbutanamide is known for its potential use as a pharmaceutical intermediate, particularly in the synthesis of certain drugs. It is characterized by a butanamide group, which includes a four-carbon chain with an amide group at the end, and a phenyl group attached to the second carbon. The N-methyl group indicates that there is a methyl group attached to the nitrogen atom in the amide. Due to its specific structure, it can be involved in various chemical reactions and has been studied for its potential therapeutic properties.

4871-04-9

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4871-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4871-04-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4871-04:
(6*4)+(5*8)+(4*7)+(3*1)+(2*0)+(1*4)=99
99 % 10 = 9
So 4871-04-9 is a valid CAS Registry Number.

4871-04-9Downstream Products

4871-04-9Relevant academic research and scientific papers

Photocatalytic Hydromethylation and Hydroalkylation of Olefins Enabled by Titanium Dioxide Mediated Decarboxylation

Zhu, Qilei,Nocera, Daniel G.

, p. 17913 - 17918 (2020/12/04)

A versatile method for the hydromethylation and hydroalkylation of alkenes at room temperature is achieved by using the photooxidative redox capacity of the valence band of anatase titanium dioxide (TiO2). Mechanistic studies support a radical-based mechanism involving the photoexcitation of TiO2 with 390 nm light in the presence of acetic acid and other carboxylic acids to generate methyl and alkyl radicals, respectively, without the need for stoichiometric base. This protocol is accepting of a broad scope of alkene and carboxylic acids, including challenging ones that produce highly reactive primary alkyl radicals and those containing functional groups that are susceptible to nucleophilic substitution such as alkyl halides. This methodology highlights the utility of using heterogeneous semiconductor photocatalysts such as TiO2 for promoting challenging organic syntheses that rely on highly reactive intermediates.

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