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Ethyl-2-amino-3-(4'-chlorophenyl)prop-2-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

204859-64-3

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204859-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 204859-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,8,5 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 204859-64:
(8*2)+(7*0)+(6*4)+(5*8)+(4*5)+(3*9)+(2*6)+(1*4)=143
143 % 10 = 3
So 204859-64-3 is a valid CAS Registry Number.

204859-64-3Downstream Products

204859-64-3Relevant academic research and scientific papers

54. A New Azepine-Ring Synthesis

Kvita, Vratislav,Sauter, Hanspeter,Rihs, Grety

, p. 457 - 463 (1989)

A new one-step synthesis of an azepine ring is described.The 2H-pyran-2-one ring of methyl cumalate (8) or cumalaldehyde (2) upon reaction with an 1-aminoacryl derivative, e.g. 1 or 6, is opened with subsequent decarboxylation to give a 1-aminobutadiene d

A novel synthesis of didehydroamino acid esters from azomethine ylides

Groundwater, Paul W.,Sharif, Toqir,Arany, Andrea,Hibbs, David E.,Hursthouse, Michael B.,Garnett, Ian,Nyerges, Miklos

, p. 2837 - 2846 (2007/10/03)

A novel synthesis of didehydroamino acid (DDAA) esters 5 is described, starting from aldimines 2. The mechanism for this reaction has been shown to involve the cycloaddition of an azomethine ylide 3 to an imine 2, followed by the base-catalysed ring-opening of the resulting imidazolidine intermediate 7. This novel method has also been extended to the synthesis of DDAA esters 5 catalysed by imines.

A new synthesis of didehydroamino acid esters

Groundwater, Paul W.,Sharif, Toqir,Arany, Andrea,Hibbs, David E.,Hursthouse, Michael B.,Nyerges, Miklos

, p. 1433 - 1436 (2007/10/03)

A novel synthesis of didehydroamino acid (DDAA) esters 4 is described, starting from aldimines 1. The mechanism for this reaction involves the cycloaddition of an azomethine ylide 2 to an imine 1, followed by the base-catalysed ring-opening of the imidazolidine intermediate 6. This method has also been extended to the synthesis of DDAA esters 4h-j catalysed by an imine 1a.

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