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7-cyclohexyl-2-methyl-5,6-diphenyl-3,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1242317-68-5

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1242317-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1242317-68-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,3,1 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1242317-68:
(9*1)+(8*2)+(7*4)+(6*2)+(5*3)+(4*1)+(3*7)+(2*6)+(1*8)=125
125 % 10 = 5
So 1242317-68-5 is a valid CAS Registry Number.

1242317-68-5Downstream Products

1242317-68-5Relevant academic research and scientific papers

Novel antiviral compounds against gastroenteric viral infections

Mohamed, Mosaad S.,El-Hameed, Rania H. Abd,Sayed, Amira I.,Soror, Sameh H.

, p. 194 - 205 (2015)

Viral gastroenteritis is a serious viral infection which affects a large number of individuals around the world, most of them being children. The infection may occur due to different viruses, for example, coxsackievirus, adenovirus, and rotavirus. There i

Design, synthesis, assessment, and molecular docking of novel pyrrolopyrimidine (7-deazapurine) derivatives as non-nucleoside hepatitis C virus NS5B polymerase inhibitors

Mohamed, Mosaad S.,Sayed, Amira I.,Khedr, Mohammed A.,Soror, Sameh H.

, p. 2146 - 2157 (2016/04/20)

Hepatitis C virus (HCV) infection is highly persistent and presents an unmet medical need requiring more effective treatment options. This has spurred intensive efforts to discover novel anti-HCV agents. The RNA-dependent RNA polymerase (RdRp), NS5B of HC

Synthesis of pyrrolo[2,3-d]pyrimidin-4-ones(7-deazapurines) under solvent- and catalyst-free conditions

Davoodnia,Bakavoli,Khashi,Moloudi,Tavakoli-Hoseini

experimental part, p. 4625 - 4628 (2010/11/16)

A facile one-pot synthesis of some new 3,7-dihydro-4H-pyrrolo[2,3- d]pyrimidin-4-ones in good yields has been developed through cyclocondensation of 2-amino-1H-pyrrole-3-carboxamides with triethyl orthoesters in solvent- and catalyst-free conditions.

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