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7-Benzyl-1-methylhypoxanthine is a chemical compound with the molecular formula C12H11N5O. It is a derivative of hypoxanthine, a naturally occurring purine nucleoside, and features a benzyl group attached to the 7th carbon and a methyl group at the 1st nitrogen position. 7-benzyl-1-methylhypoxanthine is of interest in medicinal chemistry and pharmacology due to its potential as a precursor in the synthesis of various biologically active molecules, such as adenosine receptor agonists and antagonists, which play a role in regulating physiological processes like blood flow, heart rate, and neurotransmission. The specific structure of 7-benzyl-1-methylhypoxanthine may also influence its binding affinity and selectivity for different adenosine receptor subtypes, making it a valuable compound for research in drug development and understanding receptor-ligand interactions.

7781-38-6

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7781-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7781-38-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7781-38:
(6*7)+(5*7)+(4*8)+(3*1)+(2*3)+(1*8)=126
126 % 10 = 6
So 7781-38-6 is a valid CAS Registry Number.

7781-38-6Upstream product

7781-38-6Downstream Products

7781-38-6Relevant academic research and scientific papers

Purines. LX. Dimroth rearrangement and concomitant hydrolytic deamination of 7-alkyl-1-methyladenines

Fujii,Saito,Ii,Suzuki

, p. 382 - 384 (1994)

The Dimroth rearrangement of 7-alkyl-1-methyladenines (8) to produce 7- alkyl-N6-methyladenines (9) (63-72% yield) has been found to be accompanied with unusual hydrolytic deaminations to give 7-alkyl-1-methyl-hypoxanthines (10) (1-3.5%) and/or 7-alkylhypoxanthines (11) (12-22%), when effected in boiling H2O for 4-70 h. Probable pathways leading to these by-products are proposed.

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