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(E)-1-(3-Pyridyl)ethanone O-acetyl oxime is a chemical compound with the molecular formula C9H11NO2. It is an oxime derivative of (E)-1-(3-pyridyl)ethanone, where the hydroxyl group of the oxime is acetylated. (E)-1-(3-Pyridyl)ethanone O-acetyl oxime is characterized by its yellow crystalline appearance and is soluble in common organic solvents. It is synthesized by reacting (E)-1-(3-pyridyl)ethanone with hydroxylamine and then acetylating the resulting oxime with acetic anhydride. (E)-1-(3-Pyridyl)ethanone O-acetyl oxime has potential applications in the field of organic chemistry, particularly as an intermediate in the synthesis of various pharmaceuticals and agrochemicals.

3240-21-9

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3240-21-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3240-21-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,4 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3240-21:
(6*3)+(5*2)+(4*4)+(3*0)+(2*2)+(1*1)=49
49 % 10 = 9
So 3240-21-9 is a valid CAS Registry Number.

3240-21-9Downstream Products

3240-21-9Relevant academic research and scientific papers

Copper(0)/PPh3-Mediated Bisheteroannulations of o-Nitroalkynes with Methylketoximes Accessing Pyrazo-Fused Pseudoindoxyls

Meng, Huanxin,Xu, Zhenhua,Qu, Zhonghua,Huang, Huawen,Deng, Guo-Jun

supporting information, p. 6117 - 6121 (2020/08/12)

A copper(0)/PPh3-mediated cascade bisheteroannulation reaction of o-nitroalkynes with methylketoximes has been developed that provides viable access to a diverse range of pyrazo-fused pseudoindoxyl compounds. Synthetically useful functional groups including sensitive C-I bonds are compatible with this system. Mechanistic studies suggest a reaction cascade involving sequential PPh3-mediated deoxygenative cycloisomerization and copper-catalyzed [3 + 2] pyrazo-annulation.

Cu-Catalyzed Coupling of O-Acyl Oximes with Isatins: Domino Rearrangement Strategy for Direct Access to Quinoline-4-Carboxamides by C–N Bond Cleavage

Ramaraju, Andhavaram,Chouhan, Neeraj Kumar,Ravi, Owk,Sridhar, Balasubramanian,Bathula, Surendar Reddy

, p. 2963 - 2971 (2018/06/27)

A mild domino rearrangement strategy for the direct access to substituted quinoline-4-carboxamides has been developed. This copper-catalyzed coupling reaction of O-acyl oximes with isatins in the presence of molecular oxygen as the sole oxidizing agent proceeds through a ring expansion of the isatins through cleavage of the two C–N bonds.

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