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4-Phenylbutadiynyl-morpholine is a chemical compound with the molecular formula C12H11NO. It is a derivative of morpholine, an organic compound with a five-membered ring containing two oxygen atoms and two carbon atoms. The compound features a 4-phenylbutadiynyl group, which consists of a phenyl ring (a benzene ring with a hydrogen atom replaced by a phenyl group) attached to a butadiynyl chain (a four-carbon chain with triple bonds between the carbon atoms). This unique structure gives 4-phenylbutadiynyl-morpholine potential applications in various fields, such as pharmaceuticals, materials science, and chemical research. The compound is known for its stability and reactivity, making it a valuable intermediate in the synthesis of more complex molecules.

4282-94-4

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4282-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4282-94-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,8 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4282-94:
(6*4)+(5*2)+(4*8)+(3*2)+(2*9)+(1*4)=94
94 % 10 = 4
So 4282-94-4 is a valid CAS Registry Number.

4282-94-4Downstream Products

4282-94-4Relevant academic research and scientific papers

Palladium-catalyzed coupling of (1,3-butadiynyl)amines with aryl and vinyl iodides

Loffler,Himbert

, p. 232 - 233 (2007/10/02)

4-Aryl, 4-heteroaryl- and 4-vinyl substituted (1,3-butadiynyl)-amines 7 and 8 are prepared in a one-pot synthesis by the successive treatment of the (3,4,4-trichloro-3-buten-1-ynyl)amines 1 with two equivalents of butyllithium and zinc chloride and by the palladium-catalyzed cross-coupling of the resulting aminobutadiynylzinc chlorides 4 with alkenyl, aryl and heteroaryl iodides, respectively.

A New Pathway to (4-Aryl-1,3-butadiynyl)amines

Loeffler, Achim,Himbert, Gerhard

, p. 125 - 126 (2007/10/02)

(4-Aryl-1,3-butadiynyl)amines 5 are prepared in a two-step synthesis: Palladium(II) catalyzed cross-coupling of arylacetylenes 1 and 2-bromo-1,1-dichloroethene (2) furnishes the 4-aryl-1,1-dichloro-1-buten-3-ynes 3, which are transformed into 5 by two equ

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