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2-(4-chlorophenyl)-N,N-dimethylpropanamide is a chemical compound with the molecular formula C11H14ClNO. It is a derivative of propanamide, featuring a 4-chlorophenyl group attached to the 2-position of the propanamide backbone. 2-(4-chlorophenyl)-N,N-dimethylpropanamide is an organic molecule that belongs to the class of amides, characterized by the presence of a carbonyl group (C=O) bonded to a nitrogen atom. The N,N-dimethyl groups indicate that two methyl groups are attached to the nitrogen atom, which can influence the compound's polarity and solubility properties. This specific chemical structure may be relevant in various applications, such as pharmaceuticals or chemical research, due to its potential to form hydrogen bonds and its lipophilic nature.

1949-36-6

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1949-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1949-36-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,4 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1949-36:
(6*1)+(5*9)+(4*4)+(3*9)+(2*3)+(1*6)=106
106 % 10 = 6
So 1949-36-6 is a valid CAS Registry Number.

1949-36-6Downstream Products

1949-36-6Relevant academic research and scientific papers

Palladium-Catalyzed Hydrocarbonylative C-N Coupling of Alkenes with Amides

Zhou, Xibing,Zhang, Guoying,Gao, Bao,Huang, Hanmin

supporting information, p. 2208 - 2212 (2018/04/30)

An efficient palladium-catalyzed hydrocarbonylative C-N coupling of alkenes with amides has been developed. The reaction was performed via hydrocarbonylation of alkenes, followed by acyl metathesis with amides. Both intermolecular and intramolecular react

Pd-Catalyzed Site-Selective p-Hydroxyphenyloxylation of Benzylic α-C(sp3)-H Bonds with 1,4-Benzoquinone

Song, Guangjun,Zheng, Ziwei,Wang, Yanhui,Yu, Xinhong

, p. 6002 - 6005 (2016/12/09)

A Pd-catalyzed, site-selective p-hydroxyphenyloxylation of benzylic α-C(sp3)-H bonds with 1,4-benzoquinone using thioamide as a directing group is reported. 1,4-Benzoquinone is employed as the p-hydroxyphenyloxy source without extra oxidants. T

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