15837-08-8 Usage
Description
2,6-DIHYDROXY-3,9-DIMETHYLPURINE is a purine derivative characterized by the presence of two hydroxyl groups at the 2nd and 6th positions and two methyl groups at the 3rd and 9th positions. It is a heterocyclic compound with potential applications in various fields due to its unique chemical structure and properties.
Uses
Used in Pharmaceutical Research:
2,6-DIHYDROXY-3,9-DIMETHYLPURINE is used as a research compound for studying the molecular mechanisms of various biological processes. Its unique structure allows it to interact with specific targets, making it a valuable tool in the development of new drugs and therapies.
Used in Chemical Synthesis:
2,6-DIHYDROXY-3,9-DIMETHYLPURINE can be used as a starting material or intermediate in the synthesis of more complex organic compounds, particularly those with potential applications in the pharmaceutical, agrochemical, or materials science industries.
Used in Analytical Chemistry:
Due to its unique chemical properties, 2,6-DIHYDROXY-3,9-DIMETHYLPURINE can be employed as a reference compound or standard in analytical chemistry for the calibration of instruments or the development of new analytical methods.
Used in Biochemical Studies:
2,6-DIHYDROXY-3,9-DIMETHYLPURINE may be utilized in biochemical research to investigate the interactions between purine derivatives and various biomolecules, such as enzymes, receptors, or nucleic acids. This can provide insights into the role of these compounds in cellular processes and the development of novel therapeutic strategies.
Used in the Study of Ryanodine Receptors:
2,6-DIHYDROXY-3,9-DIMETHYLPURINE is used as a tool to study the in situ activation of ryanodine receptors (RY) in pancreatic β cells from ob/ob mice. This research can contribute to a better understanding of the molecular mechanisms underlying the regulation of these receptors and their role in cellular signaling pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 15837-08-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,3 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15837-08:
(7*1)+(6*5)+(5*8)+(4*3)+(3*7)+(2*0)+(1*8)=118
118 % 10 = 8
So 15837-08-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N4O2/c1-10-3-8-4-5(12)9-7(13)11(2)6(4)10/h3H,1-2H3,(H,9,12,13)
15837-08-8Relevant articles and documents
Purines XIV. [1]. Reactivity of 8-Bromo-3,9-dimethylxanthine Towards Some Nucleophilic Reagents
Youssef, Shaker,Pfleiderer, Wolfgang
, p. 949 - 954 (1998)
The reactivity of 8-bromo-3,9-dimethylxanthine (6) towards a variety of nucleophilic reagents has been investigated. Nucleophilic displacements take place easily with aliphatic mercaptans and aliphatic alcohols, whereas aliphatic amines required more severe conditions. Prolonged heating of 6 with amines causes a new type of rearrangement from 3,9- to 3,7-dimethylxanthines due to a 1,3-sigmatropic shift of the N(9)-methyl group.
SYNTHESIS OF 3,9-DIALKYLGUANINES AND THEIR CONVERSION INTO 3-ALKYLWYES, MODELS FOR THE FLUORESCENT NUCLEOSIDES FROM PHENYLALANINE TRANSFER RIBONUCLEIC ACIDS
Itaya, Taisuke,Ogawa, Kazuo
, p. 1767 - 1774 (2007/10/02)
Synthesis of 3,9-dialkylguanines 5 has been accomplished by N-cyanation of 1-alkyl-5-(alkylamino)imidazole-4-carboxamides 3 followed by base-catalysed cyclisation.Cyclocondensation of 9-alkyl-3-methylguanines 5a, d, f with MeCOCH2Br gave 3-alkylwyes 6, model compounds of the most probable structure for wyosine from Torulopsis utilis tRNAPhe.
