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6-methyl-4-phenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1345840-60-9

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1345840-60-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1345840-60-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,5,8,4 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1345840-60:
(9*1)+(8*3)+(7*4)+(6*5)+(5*8)+(4*4)+(3*0)+(2*6)+(1*0)=159
159 % 10 = 9
So 1345840-60-9 is a valid CAS Registry Number.

1345840-60-9Relevant academic research and scientific papers

Design, synthesis and in vitro evaluation of tetrahydropyrimidine-isatin hybrids as potential antitubercular and antimalarial agents

Akhaja, Tarunkumar Nanjibhai,Raval, Jignesh Priyakant

, p. 785 - 788 (2012)

A series of 5-substituted-3-[{5-(6-methyl-2-oxo/thioxo-4-phenyl-1,2,3,4- tetrahydropyrimidin-5-yl)-1,3,4-oxadiazol-2-yl}-imino]-1,3-dihydro-2H-indol-2- one were synthesized, characterized and screened for their anti-tubercular and antimalarial activity.

Synthesis of alkoxyphthalimide derivatized oxoimidazolidinyl oxazolo/thiazolo dihydropyrimidine and oxoimidazolidinyl tetrahydropyrimidine via common Schiff base intermediate and evaluation of their antibacterial activity

Kumawat, Monika,Kherodiya, Bhawana,Prajapat, Prakash,Talesara

, p. 117 - 127 (2015/01/30)

Synthesis of N-(2-(4-substituted phenyl)-3-(2-(1,3-dioxoisoindolin-2-yloxy)ethyl)-5-oxoimidazolidin-1-yl)-3-(2-(1,3-dioxoisoindolin-2-yloxy)ethyl)-6-methyl-2-oxo/thioxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carboxamides and N-(2-(4-substituted phenyl)-3

1,3-dihydro-2H-indol-2-ones derivatives: Design, Synthesis, in vitro antibacterial, antifungal and antitubercular study

Akhaja, Tarunkumar Nanjibhai,Raval, Jignesh Priyakant

, p. 5573 - 5579 (2011/12/21)

1,3-dihydro-2H-indol-2-ones derivatives are reported to exhibit a wide variety of biodynamic activities such as antituberculer, anti HIV, fungicidal, antibacterial, anticonvulsant. These valid observations led us to synthesize some new indole-2-one deriva

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