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2-(4-Chloro-phenyl)-N-methyl-propionamide is a chemical compound with the molecular formula C10H12ClNO. It is a derivative of propionamide, featuring a 4-chlorophenyl group at the 2-position and a methyl group attached to the nitrogen atom. 2-(4-Chloro-phenyl)-N-methyl-propionamide is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain drugs and pesticides. Its chemical structure endows it with specific properties that make it valuable in organic chemistry and medicinal chemistry research.

1949-63-9

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1949-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1949-63-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,4 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1949-63:
(6*1)+(5*9)+(4*4)+(3*9)+(2*6)+(1*3)=109
109 % 10 = 9
So 1949-63-9 is a valid CAS Registry Number.

1949-63-9Downstream Products

1949-63-9Relevant academic research and scientific papers

Synthesis of phenanthridin-3-one derivatives: Non-steroidal inhibitors of steroid 5-α-reductase

Mook Jr., Robert A.

, p. 3969 - 3972 (1995)

A short and efficient six-step synthesis of novel phenanthridin-3-one derivatives is described. The synthesis of these derivatives is highlighted by the cyclization of a suitably placed ketone side chain with a thioiminium ion. The derivatives prepared we

Reaction pathway and rate-determining step of the Schmidt rearrangement/fragmentation: A kinetic study

Akimoto, Ryo,Tokugawa, Takehiro,Yamamoto, Yutaro,Yamataka, Hiroshi

experimental part, p. 4073 - 4078 (2012/06/29)

The Schmidt rearrangement of substituted 3-phenyl-2-butanone with trimethylsilyl azide in 90% (v/v) aqueous TFA gave two types of product, fragmentation and rearrangement, the ratio of which depends on the substituent: more fragmentation for a more electron-donating substituent. Rate measurements by azotometry indicated the presence of an induction period, and the pseudo-first-order rate constants showed saturation kinetics with respect to the azide concentration. It was indicated that the reaction proceeds through pre-equilibrium in the formation of iminodiazonium (ID) ion and that the N 2 liberation from the ID ion is rate-determining. Under high azide concentration conditions, where the effective reactant is the ID ion, the reaction gave a linear Hammett plot with a value of -0.50. The observed substituent effects on the rate and the product selectivity imply that path bifurcation on the way from the rate-determining TS to the product states occurs, as suggested by previous molecular dynamics simulations, in a similar manner to the analogous Beckmann rearrangement/fragmentation reactions.

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