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3-Benzyl-5,7-dimethyl-2-thioxo-2,3-dihydro-1H-pyrido[2,3-d]pyrimidin-4-one is a complex organic compound belonging to the pyrido[2,3-d]pyrimidine family. This molecule features a pyrido[2,3-d]pyrimidin-4-one core structure, which is a fused ring system consisting of a pyridine and a pyrimidine. The compound is characterized by a benzyl group attached to the 3-position, two methyl groups at the 5 and 7 positions, and a thioxo group at the 2-position, which together contribute to its unique chemical properties. The 2,3-dihydro indicates the presence of two hydrogen atoms attached to the carbon atoms at positions 2 and 3, which are part of a saturated ring. 3-Benzyl-5,7-dimethyl-2-thioxo-2,3-dihydro-1H-pyrido[2,3-d]pyrimidin-4-one is of interest in medicinal chemistry due to its potential biological activities and may be involved in the synthesis of pharmaceuticals or as a research tool in studying the structure-activity relationships of related compounds.

1913-66-2

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1913-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1913-66-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1913-66:
(6*1)+(5*9)+(4*1)+(3*3)+(2*6)+(1*6)=82
82 % 10 = 2
So 1913-66-2 is a valid CAS Registry Number.

1913-66-2Downstream Products

1913-66-2Relevant academic research and scientific papers

Pyridopyrimidines: Part I--Synthesis and Biological Activity of 2-Thiopyridopyrimidin-4(3H)-ones

Dave, C. G.,Shah, P. R.,Desai, V. B.,Srinivasan, S.

, p. 750 - 752 (2007/10/02)

3,5,7-Trisubstituted 2-thiopyridopyrimidin-4(3H)-ones (IV) have been synthesized by condensation of 2-amino-3-carbethoxy-4,6-disubstituted-pyridines (I) with a variety of isothiocyanates (II) followed by cyclization of the resultant thioureas (III).Some of the synthesized N1-substituted-N2--thioureas (III) and IV have been tested for antibacterial and antihistaminic activities.

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