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4H-Pyrazolo[3,4-d]pyrimidin-4-one, 1,5,6,7-tetrahydro-3-phenyl-6-thioxo, is a complex organic compound belonging to the pyrazolo[3,4-d]pyrimidine family. This heterocyclic compound features a pyrazole ring fused to a pyrimidine ring, with a phenyl group attached to the 3-position and a thioxo group at the 6-position. The compound is characterized by its 1,5,6,7-tetrahydro structure, indicating the presence of four hydrogen atoms bonded to the carbon atoms in these positions. This specific arrangement of atoms and functional groups endows the compound with unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

42754-80-3

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42754-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42754-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,7,5 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 42754-80:
(7*4)+(6*2)+(5*7)+(4*5)+(3*4)+(2*8)+(1*0)=123
123 % 10 = 3
So 42754-80-3 is a valid CAS Registry Number.

42754-80-3Relevant academic research and scientific papers

Synthesis of some new pyrazole and pyrazolopyrimidine derivatives [1]

Ghozlan, Said A. S.,Abdelrazek, Fathy M.,Mohamed, Mona H.,Azmy, Khaled E.

experimental part, p. 1379 - 1385 (2011/02/23)

A series of pyrazolo [3,4-d] pyrimidine, pyrazolo [1,5-a] pyrimidine, and pyrazolyl triazoles have been prepared via reaction of ethyl 5-amino-3-phenylpyrazole-4-carboxylate with isothiocyanic esters, α,β-unsaturated nitriles, and some active methylene re

Guanosine Analogues. Synthesis of Nucleosides of Certain 3-Substituted 6-Aminopyrazolopyrimidin-4(5H)-ones as Potential Immunotherapeutic Agents

Bontems, Roger J.,Anderson, Jack D.,Smee, Donald F.,Jin, Ai,Alaghamandan, Hassan A.,et al.

, p. 2174 - 2178 (2007/10/02)

Several guanosine analogues were synthesized in the pyrazolopyrimidine ring system with various substituents at the 3-position.The new analogues prepared here include the CH3 (2-amino-3-methyl-1-β-D-ribofuranosylpyrazolopyrimidin-4(5H)-one,

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