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1-(4-chlorophenyl)-3-(pyridin-3-yl)propan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1544040-98-3

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1544040-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1544040-98-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,4,4,0,4 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1544040-98:
(9*1)+(8*5)+(7*4)+(6*4)+(5*0)+(4*4)+(3*0)+(2*9)+(1*8)=143
143 % 10 = 3
So 1544040-98-3 is a valid CAS Registry Number.

1544040-98-3Downstream Products

1544040-98-3Relevant academic research and scientific papers

Rhodium-catalyzed alkylation of ketones and alcohols with alcohols

Yu,Wang,Wu,Wang

, p. 178 - 183 (2016)

An efficient method for direct alkylation of ketones and alcohols through the borrowing hydrogen strategy in the presence of rhodium complexes as catalyst was developed. This transformation is tolerant to various functional substrates and is efficient in C-C coupling of primary and secondary alcohols, which provides an alternative method of the synthesis of functional ketones from simple and commercially available materials.

Synthesis of β-heteroaryl carbonyl compounds via direct cross-coupling of allyl alcohols with heteroaryl boronic acids under cooperative bimetallic catalysis

Zhu, Mingxiang,Du, Hongli,Li, Jingya,Zou, Dapeng,Wu, Yusheng,Wu, Yangjie

supporting information, p. 1352 - 1355 (2018/03/06)

The eco-friendly cooperative Cu/Pd-catalyzed oxidative Heck reaction of allyl alcohols with heteroaryl boronic acids under air was described. The ready availability of starting materials and the mild reaction conditions made this protocol a safe and operationally convenient strategy for the efficient synthesis of β-heteroaryl carbonyl compounds.

Iridium-CNP complex catalyzed cross-coupling of primary alcohols and secondary alcohols by a borrowing hydrogen strategy

Wang, Dawei,Zhao, Keyan,Yu, Xin,Miao, Hongyan,Ding, Yuqiang

, p. 42924 - 42929 (2015/02/19)

A highly efficient C-C bond formation has been developed through the cross-coupling of primary and secondary alcohols. The corresponding functionalized ketones were obtained with an iridium-CNP complex as a catalyst through the borrowing hydrogen strategy. The present methodology provides an easy alternative method to aldol reaction derivatives. More importantly, the complexes were also effective catalysts for the alkylation of an aromatic amine with a tertiary alkyl amine. This journal is

Direct α-alkylation of ketones with primary alcohols catalyzed by iridium-CNP complex

Wang, Dawei,Zhao, Keyan,Ma, Piming,Xu, Chongying,Ding, Yuqiang

supporting information, p. 7233 - 7235 (2015/01/09)

The α-alkylation of ketones with primary alcohols was realized by CC cross-coupling with iridium-CNP complexes as catalyst. This reaction proceeds via dehydrogenation reactions, aldol condensation, and hydrogenation using the borrowed hydrogen atoms from alcohols. The pyridyl methanols and other heterocyclic substituted methanols, especially alkyl alcohols, were also suitable for this transformation.

Efficient ruthenium-catalyzed α-alkylation of ketones using pyridyl methanols

Yan, Feng-Xia,Zhang, Min,Wang, Xiao-Ting,Xie, Feng,Chen, Meng-Meng,Jiang, Huanfeng

supporting information, p. 1193 - 1198 (2014/02/14)

By employing an easily available [Ru(p-cymene)Cl2] 2/Xantphos/t-BuOK catalyst system, the α-alkylation of ketones was demonstrated by using pyridyl methanol as the alkylating reagents. The synthetic protocol allows synthesizing a wid

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