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2-phenyl-N-(3-phenylprop-2-yn-1-yl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1333470-29-3

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1333470-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1333470-29-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,4,7 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1333470-29:
(9*1)+(8*3)+(7*3)+(6*3)+(5*4)+(4*7)+(3*0)+(2*2)+(1*9)=133
133 % 10 = 3
So 1333470-29-3 is a valid CAS Registry Number.

1333470-29-3Downstream Products

1333470-29-3Relevant academic research and scientific papers

Consecutive three-component synthesis of (hetero)arylated propargyl amides by chemoenzymatic aminolysis-Sonogashira coupling sequence

Hassan, Sidra,Ullrich, Anja,Müller, Thomas J. J.

supporting information, p. 1571 - 1576 (2015/01/30)

A novel chemoenzymatic three-component synthesis of (hetero)arylated propargyl amides in good yields based upon Novozyme 435 (Candida antarctica lipase B (CAL-B)) catalyzed aminolysis of methyl carboxylates followed by Sonogashira coupling with (hetero)aryliodides in a consecutive one-pot fashion has been presented. This efficient methodology can be readily concatenated with a CuAAC (Cu catalyzed alkyne azide cycloaddition) as a third consecutive step to furnish 1,4-disubstituted 1,2,3-triazole ligated arylated propargyl amides. This one-pot process can be regarded as a transition metal catalyzed sequence that takes advantage of the copper source still present from the cross-coupling step.

Gold-catalyzed cyclization of nonterminal propargylic amides to substituted alkylideneoxazolines and-oxazines

Hashmi, A. Stephen K.,Schuster, Andreas M.,Schmuck, Martin,Rominger, Frank

supporting information; experimental part, p. 4595 - 4602 (2011/10/03)

The substrate scope of the gold-catalyzed cyclization of nonterminal propargylic amides to oxazolines and oxazines was investigated. Sixteen alkyl-substituted and 35 aryl-substited substrates were prepared by a very variable route from trimethylsilyl-(TMS

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