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(2E,3E)-3-methyl-4-phenylbut-3-en-2-one O-acetyl oxime is a chemical compound with the molecular formula C13H13NO2. It is an oxime derivative of the enone (2E,3E)-3-methyl-4-phenylbut-3-en-2-one, where the oxime group is formed by the addition of hydroxylamine to the carbon-carbon double bond. The O-acetyl group is attached to the oxime nitrogen, resulting in an acetamide functional group. (2E,3E)-3-methyl-4-phenylbut-3-en-2-one O-acetyl oxime is characterized by its conjugated diene system, which contributes to its chemical reactivity and potential applications in organic synthesis. It is an example of a chiral molecule, with the potential for different enantiomeric forms due to the presence of a chiral center. The compound's structure and properties make it a subject of interest in the field of organic chemistry, particularly for its potential use in the synthesis of more complex molecules and its study in understanding the behavior of chiral compounds.

1722-74-3

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1722-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1722-74-3 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 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1722-74:
(6*1)+(5*7)+(4*2)+(3*2)+(2*7)+(1*4)=73
73 % 10 = 3
So 1722-74-3 is a valid CAS Registry Number.

1722-74-3Downstream Products

1722-74-3Relevant 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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