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(E)-2-(4-(dimethylamino)benzylidene)butanal is an organic compound characterized by its molecular formula C13H17NO. It is a derivative of butanal, featuring a benzylidene group attached to the 2-position, with a 4-(dimethylamino)benzyl moiety. (E)-2-(4-(dimethylamino)benzylidene)butanal is known for its distinct chemical structure, which includes a double bond (E-configuration) between the 2- and 3-positions, and a dimethylamino group on the benzene ring. It is often used in the synthesis of various pharmaceuticals and chemical compounds due to its unique reactivity and functional groups.

87234-34-2

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87234-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87234-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,3 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87234-34:
(7*8)+(6*7)+(5*2)+(4*3)+(3*4)+(2*3)+(1*4)=142
142 % 10 = 2
So 87234-34-2 is a valid CAS Registry Number.

87234-34-2Downstream Products

87234-34-2Relevant academic research and scientific papers

Direct β-C(sp3)-H Functionalization of Aliphatic Amines to α,β-Unsaturated Imines, Aldehydes, and Chromenes

Mandal, Sumana,Mahato, Sujit,Jana, Chandan K.

supporting information, p. 3762 - 3765 (2015/08/18)

A metal-free method for direct β-C(sp3)-H functionalization of aliphatic amine was developed. The method is based on a reaction that yields enamine directly from the corresponding aliphatic amine, which otherwise requires the aid of metallic reagent and/or external oxidant. The reaction is operationally simple, general, and highly efficient in functionalizing both cyclic and acyclic amines. Structurally diverse unsaturated imines were obtained from N-heterocycles, while acyclic amines provided 2-alkyl cinnamaldehyde and benzopyran derivatives with excellent E/Z-selectivity.

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