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N-(4-fluorobenzyl)pyrimidin-2-amine is a chemical compound with the molecular formula C11H10FN3. It is a derivative of pyrimidin-2-amine, featuring a 4-fluorobenzyl group attached to the nitrogen atom. N-(4-fluorobenzyl)pyrimidin-2-amine is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its structure allows for the exploration of structure-activity relationships in drug design, as the fluorine atom can significantly influence the compound's pharmacokinetic and pharmacodynamic properties. The compound is also of interest in the development of new materials and as a research tool in organic synthesis.

458-74-2

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458-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 458-74-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 458-74:
(5*4)+(4*5)+(3*8)+(2*7)+(1*4)=82
82 % 10 = 2
So 458-74-2 is a valid CAS Registry Number.

458-74-2Relevant academic research and scientific papers

Research on antibacterial and antifungal agents. XI. Synthesis and antimicrobial activity of N-heteroaryl benzylamines and their schiff bases

Fioravanti,Biava,Porretta,Landolfi,Simonetti,Villa,Conte,Porta-Puglia

, p. 123 - 132 (1995)

The synthesis and antimicrobial activity of new N-heteroaryl benzylamines and their Schiff bases are reported. Antifungal data were compared with those obtained with miconazole, ketoconazole, enilconazole and imazalil sulfate, which showed that some of the tested compounds possessed moderate activity against strains of Candida albicans, Candida Sp and good activity against isolates of plant pathogenic fungi. In contrast the synthesized compounds showed poor antibacterial activity, except for 3j which exhibited abetter activity than nalidixic acid used as positive control. The results obtained are discussed on the basis of structure-activity relationships.

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