101072-05-3 Usage
Molecular Structure
1H-Purine-2,6-dione, 8-bromo-3,7-dihydro-3-methyl-7-(1-methyl-2-oxo-2-phenylethyl)contains a purine ring, which is a bicyclic structure consisting of a six-membered pyrimidine ring fused to a five-membered imidazole ring. The purine ring is the backbone of many important biomolecules, such as nucleotides and nucleic acids.
Bromo Substitution
The purine ring has an 8-bromo substitution, which means a bromine atom is attached to the carbon at position 8 of the purine ring. This substitution can significantly affect the compound's chemical properties and biological activity.
Side Chain
The compound has a 3,7-dihydro-3-methyl-7-(1-methyl-2-oxo-2-phenylethyl) side chain attached to the purine ring. This side chain consists of a 3-methyl group, a 7-dihydro ring, and a 1-methyl-2-oxo-2-phenylethyl group. The presence of this side chain can influence the compound's solubility, stability, and interaction with biological targets.
Potential Biological Activity
Due to its complex structure, 1H-Purine-2,6-dione, 8-bromo-3,7-dihydro-3-methyl-7-(1-methyl-2-oxo-2-phenylethyl)may exhibit biological activity, making it of interest for medicinal chemistry research. The specific biological activity will depend on the interactions between the compound and various biomolecules, such as enzymes, receptors, or nucleic acids.
Applications in Drug Development
The compound's potential biological activity may lead to its use in drug development, as it could serve as a lead compound for the design of new therapeutic agents. Researchers may modify the structure of the compound to optimize its activity, selectivity, and pharmacokinetic properties.
Chemical Tool for Studying Biological Processes
1H-Purine-2,6-dione, 8-bromo-3,7-dihydro-3-methyl-7-(1-methyl-2-oxo-2-phenylethyl)could also be used as a chemical tool to study specific biological processes, such as enzyme inhibition or modulation of receptor activity. By understanding how the compound interacts with biological targets, researchers can gain insights into the underlying mechanisms of various diseases and develop targeted therapies.
Safety Precautions
Due to the complex structure and potential biological activity of 1H-Purine-2,6-dione, 8-bromo-3,7-dihydro-3-methyl-7-(1-methyl-2-oxo-2-phenylethyl)-, it is essential to handle the compound with care and follow appropriate safety precautions. This may include using appropriate personal protective equipment, working in a well-ventilated area, and following proper disposal procedures for waste materials.
Check Digit Verification of cas no
The CAS Registry Mumber 101072-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,7 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 101072-05:
(8*1)+(7*0)+(6*1)+(5*0)+(4*7)+(3*2)+(2*0)+(1*5)=53
53 % 10 = 3
So 101072-05-3 is a valid CAS Registry Number.
