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6-Benzyl-7-chloro-5-methyl-pyrido[2,3-d]pyrimidine-2,4-diamine is a complex organic compound with the molecular formula C16H14ClN5. It belongs to the class of pyrido[2,3-d]pyrimidines, which are fused heterocyclic compounds with a pyridine and a pyrimidine ring. This specific compound features a benzyl group at the 6th position, a chlorine atom at the 7th position, and a methyl group at the 5th position. The 2,4-diamine functional group is present at the 2nd and 4th positions of the pyrimidine ring. 6-benzyl-7-chloro-5-methyl-pyrido[2,3-d]pyrimidine-2,4-diamine may have potential applications in medicinal chemistry, particularly as a precursor or intermediate in the synthesis of biologically active molecules. Its chemical structure and properties make it a subject of interest for researchers exploring new drug candidates or other chemical entities with specific therapeutic or chemical functionalities.

4871-68-5

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4871-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4871-68-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4871-68:
(6*4)+(5*8)+(4*7)+(3*1)+(2*6)+(1*8)=115
115 % 10 = 5
So 4871-68-5 is a valid CAS Registry Number.

4871-68-5Downstream Products

4871-68-5Relevant academic research and scientific papers

NAD+-dependent DNA ligase inhibitors

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Page/Page column 10, (2008/06/13)

Disclosed herein are pyrido[2,3-d]pyrimidines having the structure wherein R1, and R2 are independently selected from nitro and amino; wherein R3 is selected from alkyl (C1-C10) and cycloalkyl (C3-C8); wherein R4 is selected from hydrogen, benzyl, alkyl (C1-C10), cycloalkyl (C3-C8), arylalkyl (C4-C8), and aryl (C3-C8); wherein R5 and R6 are independently selected from hydrogen, benzyl, alkyl (C1-C10), cycloalkyl (C3-C8), arylalkyl (C4-C14), and aryl (C3-C8); wherein R3 and R4 may form a ring; wherein R5 and R6 may form a ring or a heterocyclic structure; and wherein R5 and R6 are independently unsubstituted or substituted, wherein each substituent is independently selected from halogen, amino, alkyl (C1-C6), haloalkyl (C1-C6), alkoxy(C1-C6), alkylenedioxy, aryl, heteroaryl, and cycloalkyl (C3-C8). Also disclosed are methods for the preparation of compounds of Formula I and various intermediates. These compounds are useful as NAD+-dependent DNA ligase inhibitors.

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