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2-ButenaMide, N-Methyl-, (2E)-, also known as N-Methyl-2-butenamide or (2E)-N-methylbut-2-enamide, is an organic compound characterized by its molecular formula C5H9NO. 2-ButenaMide, N-Methyl-, (2E)- features a 2-butenamide backbone with a methyl group attached to the nitrogen atom. The (2E)- notation indicates that the molecule has a trans double bond between the second and third carbon atoms. It is a colorless liquid with a pungent odor and is used in various chemical reactions and as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Due to its reactivity, it is important to handle 2-ButenaMide, N-Methyl-, (2E)- with care, following proper safety protocols.

1189-03-3

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1189-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1189-03-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1189-03:
(6*1)+(5*1)+(4*8)+(3*9)+(2*0)+(1*3)=73
73 % 10 = 3
So 1189-03-3 is a valid CAS Registry Number.

1189-03-3Downstream Products

1189-03-3Relevant academic research and scientific papers

Synthesis of 2,3-dihydroxy-3-(N-substituted carbamoyl)propylphosphonic acid derivatives as hybrid DOXP-fosmidomycin analogues

Blatch, Gregory L.,Kaye, Perry T.,Klein, Rosalyn,Lobb, Kevin A.,Mutorwa, Marius K.

, (2022/02/05)

A six-step synthetic pathway has been established to access a series of racemic 2,3-dihydroxy-3-(N-substituted carbamoyl)propylphosphonic acid derivatives, designed to contain structural features common to both the natural substrate 1-deoxy-D-xylulose 5-p

Ruthenium-catalyzed reduction of N-alkoxy- and N-hydroxyamides

Fukuzawa, Hiroko,Ura, Yasuyuki,Kataoka, Yasutaka

experimental part, p. 3643 - 3648 (2011/12/02)

A ruthenium-catalyzed reduction of N-alkoxy- and N-hydroxyamides was found to afford corresponding amides in good to high yields. A simple RuCl 3/Zn-Cu/alcohol system, without the addition of any other ligands, exhibited a high catalytic activity, and therefore the present reaction does not require a stoichiometric amount of metals or metal complexes as reductants. When β-substituted-α,β-unsaturated N-methoxyamides were employed as substrates, concurrent hydrogenation of the olefin moiety proceeded slowly with deprotection of the methoxy group. In the reduction of N-hydroxyamides, the alcoholic solvent was found to function as a hydrogen donor.

Synthesis of β,γ-unsaturated primary amides from α,β-unsaturated acids and investigation of the mechanism

Theodorou, Vassiliki,Gogou, Marina,Philippidou, Maria,Ragoussis, Valentine,Paraskevopoulos, Georgios,Skobridis, Konstantinos

experimental part, p. 5630 - 5634 (2011/08/22)

α,β-Unsaturated acids, through their acid chlorides, react with tritylamine in the presence of triethylamine under mild conditions, to afford in high yield and high regioselectivity the corresponding β,γ- unsaturated tritylamides. Detritylation with TFA generates quantitatively β,γ-unsaturated primary amides. An investigation of this deconjugative isomerization was performed.

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