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9-Benzyl-6-pyrrolidin-1-yl-9H-purine is a complex organic compound belonging to the purine family, characterized by a unique molecular structure. It consists of a purine core, with a benzyl group attached at the 9th position and a pyrrolidin-1-yl group at the 6th position. 9-benzyl-6-pyrrolidin-1-yl-9H-purine is known for its potential applications in medicinal chemistry, particularly as a precursor or intermediate in the synthesis of various biologically active molecules, such as adenosine receptor agonists and antagonists. Due to its specific structure, it can interact with cellular receptors, potentially influencing physiological processes. The compound's properties, such as solubility and stability, can be influenced by the presence of the benzyl and pyrrolidin-1-yl groups, making it a subject of interest for further research and development in the pharmaceutical industry.

1928-92-3

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1928-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1928-92-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,2 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1928-92:
(6*1)+(5*9)+(4*2)+(3*8)+(2*9)+(1*2)=103
103 % 10 = 3
So 1928-92-3 is a valid CAS Registry Number.

1928-92-3Downstream Products

1928-92-3Relevant academic research and scientific papers

Effect of substituent structure on pyrimidine electrophilic substitution

van der Westhuyzen, Christiaan W.,Rousseau, Amanda L.,Parkinson, Christopher J.

, p. 5394 - 5405 (2008/01/07)

In an investigation into the electrophilic nitrosation reactions of a series of 4,6-disubstituted pyrimidine derivatives, a subtle interplay between the electronic nature of the C-4 and C-6 substituents and reactivity was found where these were chloro-, mono- or disubstituted amino groups. Effects such as the presence of an aryl group or two alkyl groups on the amino moiety impede the progress of the reaction despite the presence of a second activating group.

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