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4-Phenyl-3-methyl-3-butene-2-one oxime is an organic compound with the molecular formula C11H13NO. It is a derivative of 4-phenyl-3-methyl-3-buten-2-one, featuring an oxime functional group, which is an oxime of a ketone. 4-phenyl-3-methyl-3-butene-2-one oxime is characterized by the presence of a phenyl ring, a methyl group, and a carbon-carbon double bond, with the oxime group attached to the carbonyl carbon. It is a colorless to pale yellow solid and is used in the synthesis of various pharmaceuticals and chemical intermediates. The compound is known for its potential applications in the preparation of chiral ligands and catalysts, as well as in the development of new drugs and materials. Its chemical properties and reactivity are influenced by the presence of the oxime group, which can participate in various chemical reactions, such as redox processes and condensation reactions.

1721-84-2

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1721-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1721-84-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1721-84:
(6*1)+(5*7)+(4*2)+(3*1)+(2*8)+(1*4)=72
72 % 10 = 2
So 1721-84-2 is a valid CAS Registry Number.

1721-84-2Relevant academic research and scientific papers

Polysubstituted Indole Synthesis via Palladium/Norbornene Cooperative Catalysis of Oxime Esters

Liu, Jiechun,Lin, Haojiang,Jiang, Huanfeng,Huang, Liangbin

, p. 484 - 489 (2022/01/20)

Polysubstituted indoles are prevalent in pharmaceuticals, agrochemicals, and organic materials. Presented herein is the fact that polyfunctionalized indoles can be efficiently constructed from easily accessible oxime esters and aryl iodides, involving a palladium/norbornene synergistic synthesis. The reaction is enabled by a unique class of electrophiles in palladium/norbornene cooperative catalysis, which are oxime esters derived from simple ketone. The broad substrate scope and high functional group tolerance could make this method attractive for the synthesis of polysubstituted indoles.

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