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(Z)-1-phenyl-3-(piperidin-1-yl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1356541-98-4

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1356541-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1356541-98-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,6,5,4 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1356541-98:
(9*1)+(8*3)+(7*5)+(6*6)+(5*5)+(4*4)+(3*1)+(2*9)+(1*8)=174
174 % 10 = 4
So 1356541-98-4 is a valid CAS Registry Number.

1356541-98-4Downstream Products

1356541-98-4Relevant academic research and scientific papers

Tunable and Diastereoselective Br?nsted Acid Catalyzed Synthesis of β-Enaminones

Kang, Ye-Won,Cho, Yu Jin,Han, Seung Jin,Jang, Hye-Young

supporting information, p. 272 - 275 (2016/02/03)

The Br?nsted acid catalyzed Meyer-Schuster reaction of hemiaminals was studied for the stereoselective synthesis of β-enaminones. Hemiaminals were formed from propargyl aldehydes (or the oxidation of propargyl alcohols) and amines in the presence of Br?ns

Highly regioselective synthesis of cis-β-enaminones by 1,4-addition of propiolaldehydes

Shi, Wenjuan,Sun, Shaofa,Wu, Minghu,Catano, Bryant,Li, Wan,Wang, Jian,Guo, Haibing,Xing, Yalan

supporting information, p. 468 - 471 (2015/04/27)

A convenient one-pot strategy for the regioselective synthesis of cis-β-enaminones has been developed via the condensation of propiolaldehydes and amines in EtOH. This process has opened a new synthetic route to enamines in good yield. A possible reaction mechanism involving a Michael addition/enol tautomerization via a six-membered ring transition state is proposed.

Highly stereoselective synthesis of cis-β-enaminones mediated by diethyl azodicarboxylate

Xu, Xiaoliang,Du, Ping,Cheng, Dongping,Wang, Hong,Li, Xiaonian

supporting information; experimental part, p. 1811 - 1813 (2012/02/16)

Promoted by diethyl azodicarboxylate, a novel and highly stereoselective synthesis of cis-β-enaminones via oxidative dehydrogenation and hydration of the substituted propargylamines was realized. The possible mechanism was also proposed.

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