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5-Ethoxycarbonyl-3-phenyl-1,2,3,4-tetrahydropyrimidine-2-thione is a complex organic compound with the molecular formula C13H15N3O2S. It is a derivative of tetrahydropyrimidine, a heterocyclic compound with a six-membered ring containing four carbon atoms and two nitrogen atoms. The molecule features a 5-ethoxycarbonyl group (an ester of ethanoic acid), a 3-phenyl group (a phenyl ring attached to the third carbon), and a 2-thione group (a sulfur atom bonded to the second carbon). 5-ethoxycarbonyl-3-phenyl-1,2,3,4-tetrahydropyrimidine-2-thione is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals and other chemical products. Its structure and properties make it a valuable compound for studying the reactivity and behavior of tetrahydropyrimidine derivatives.

2974-15-4

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2974-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2974-15-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2974-15:
(6*2)+(5*9)+(4*7)+(3*4)+(2*1)+(1*5)=104
104 % 10 = 4
So 2974-15-4 is a valid CAS Registry Number.

2974-15-4Downstream Products

2974-15-4Relevant academic research and scientific papers

2,4-Diamino-1-thia-3-azabutadienes, intermediates in heterocyclic synthesis

Friot,Reliquet,Reliquet,Meslin

, p. 135 - 149 (2007/10/03)

2,4-Diamino-1-thia-3-azabutadienes 1 were studied. Methylation occured at sulfur and acylation at nitrogen hound to the 2 position. Alkylation by α-bromoketones gave rise to 2-amino-5-acylthiazoles. Upon treatment with acrylic dienophiles compounds 1 reac

New 1,3-diazadienes used in heterocyclic synthesis

Friot, Celine,Reliquet, Alain,Reliquet, Francoise,Meslin, Jean Claude

, p. 695 - 702 (2007/10/03)

The synthesis of dihydropyrimidines, dihydropyrimidinones and thiadiazine-1,1-dioxides starting from neutral or cationic 2-methylthio-1,3- diazadienes is described. Addition of H2S followed by loss of methanethiol led to the corresponding thiocarbonyl compounds.

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