972-62-3 Usage
Molecular Structure
1H-Purine-2,6-dione, 8-chloro-3,7-dihydro-1,3-dimethyl-7-(4-nitrophenyl)is a purine derivative with a chlorinated ring, 2,6-dione functional groups, and 1,3-dimethyl substituents, along with a nitrophenyl group attached to the purine structure.
Purine Family
1H-Purine-2,6-dione,
8-chloro-3,7-dihydro-1,3-dimethyl-7-(4-nitrophenyl)- belongs to the purine family, which is a group of organic compounds that are characterized by a double-ring structure. Purines are one of the building blocks of nucleic acids (DNA and RNA) and play a crucial role in biological processes.
Chlorinated Derivative
The presence of a chlorine atom in the compound indicates that it is a chlorinated derivative of purine. Chlorinated compounds often exhibit different properties and reactivities compared to their non-chlorinated counterparts.
2,6-Dione Functional Group
The 2,6-dione functional group is a carbonyl group (C=O) attached to two adjacent carbon atoms in a ring structure. This group contributes to the compound's chemical properties and reactivity.
1,3-Dimethyl Substituents
The compound contains two methyl groups (CH3) attached to the first and third carbon atoms of the purine ring. Methyl groups are alkyl substituents that can influence the compound's lipophilicity, solubility, and reactivity.
Nitrophenyl Group
The presence of a nitrophenyl group (a phenyl ring with a nitro group -NO2) in the compound suggests potential uses as a dye or pharmaceutical compound. Nitrophenyl groups are known for their ability to absorb and emit light, making them suitable for dye applications. Additionally, they can be used as prodrugs or active pharmaceutical ingredients.
Biological and Pharmacological Activity
The purine structure of the compound indicates potential biological and pharmacological activity. Purine derivatives are known to interact with various enzymes, receptors, and other biomolecules, which can lead to therapeutic effects or side effects.
Further Research and Experimentation
The exact properties and applications of 1H-Purine-2,6-dione,
8-chloro-3,7-dihydro-1,3-dimethyl-7-(4-nitrophenyl)- can only be determined through additional research and experimentation. This may include in vitro and in vivo testing, as well as studies on its chemical reactivity, stability, and potential drug interactions.
Check Digit Verification of cas no
The CAS Registry Mumber 972-62-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,7 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 972-62:
(5*9)+(4*7)+(3*2)+(2*6)+(1*2)=93
93 % 10 = 3
So 972-62-3 is a valid CAS Registry Number.
