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2,6-dichloro-4,8-dipiperidinopyrimido[5,4-d]pyrimidine is a complex organic compound with the molecular formula C18H24Cl2N6. It is characterized by the presence of two chlorine atoms at the 2nd and 6th positions, and two piperidine rings attached to the 4th and 8th positions of the pyrimido[5,4-d]pyrimidine core structure. 2,6-dichloro-4,8-dipiperidinopyrimido[5,4-d]pyrimidine is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various biologically active molecules. Its chemical structure allows for further functionalization and modification, making it a versatile intermediate in the development of new drugs and pharmaceuticals. The compound's specific properties, such as its solubility, stability, and reactivity, can be tailored for specific therapeutic applications, highlighting its importance in the field of drug discovery and design.

713-92-8

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713-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 713-92-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 713-92:
(5*7)+(4*1)+(3*3)+(2*9)+(1*2)=68
68 % 10 = 8
So 713-92-8 is a valid CAS Registry Number.

713-92-8Relevant academic research and scientific papers

Selective Functionalization in 2-Nitro-p-phenylenediamine : Part II - Synthesis of Derivatives of 5-(2-Thiazolylamino)benzimidazole 2-Carbamates

Rajappa, S.,Advani, B. G.,Sreenivasan, R.

, p. 536 - 538 (2007/10/02)

2-Nitro-p-phenylenediamine (1) reacts with methyl isothiocyanate to give N-methyl-thiourea (2).The unsubstituted thiourea (7) is obtained by similar addition of 1 to benzoyl isothiocyanate, followed by base-catalyzed removal of

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