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(E)-2-(4-Chloro-benzyl)-3-p-tolylamino-propenal is a complex organic compound characterized by its molecular formula C17H15ClN, which indicates the presence of 17 carbon, 15 hydrogen, 1 chlorine, and 1 nitrogen atoms. This molecule features a propenal backbone, which is a three-carbon chain with a carbon-carbon double bond and an aldehyde group at the end. The 4-chloro-benzyl group is attached to the second carbon of the propenal, providing a chlorinated aromatic ring. Additionally, a p-tolylamino group is connected to the third carbon, introducing a tolyl (methyl-phenyl) amine moiety. The "E" configuration refers to the geometric isomerism of the molecule, indicating the relative positions of the substituents around the double bond. (E)-2-(4-Chloro-benzyl)-3-p-tolylamino-propenal is likely to be found in research settings, particularly in the fields of organic chemistry and pharmaceuticals, due to its unique structure and potential reactivity.

89816-35-3

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89816-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89816-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,1 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89816-35:
(7*8)+(6*9)+(5*8)+(4*1)+(3*6)+(2*3)+(1*5)=183
183 % 10 = 3
So 89816-35-3 is a valid CAS Registry Number.

89816-35-3Relevant academic research and scientific papers

Preparation of 3-Substituted Quinolines. I. Alkylation of Malonaldehyde Dianil Derivatives

Todoriki, Reiko,Ono, Machiko,Tamura, Shinzo

, p. 4277 - 4285 (2007/10/02)

2-Substituted 1-arylamino-3-arylimino-1-propenes (III) were prepared by the reaction of N-lithio derivatives of 1-arylamino-3-arylimino-1-propenes (malonaldehyde dianil derivatives) (II) and substituted benzyl bromides. 2-Allyl and 2-(2,4-dinitrophenyl) derivatives of II were prepared by the same method.However, the alkylation failed with less reactive alkyl halides such as ethyl iodide as alkylating agents.Hydrolysis of III afforded α-substituted β-(arylamino)acroleins (IV), which afforded 3-substiuted quinolines (V) on heating with aluminium chloride.Keywords -- 2-alkyl-1-arylamino-3-arylamino-1-propene; α-alkyl-β=(arylamino)acrolein; 3-alkylquinoline; alkylation; hydrolysis; cyclodehydration

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