21314-14-7 Usage
Explanation
This indicates the compound is composed of 12 carbon atoms, 8 hydrogen atoms, 4 nitrogen atoms, and 3 oxygen atoms, providing a basic understanding of its chemical makeup.
Compound Type
Heterocyclic compound
Explanation: It consists of a molecular structure that includes a ring made of at least two different types of elements, in this case, carbon and nitrogen. This is significant because heterocyclic compounds are foundational in medicinal chemistry and organic chemistry.
Ring System
Pyrazolo-pyrimidine
Explanation: This denotes the specific arrangement of the nitrogen-containing heterocyclic ring in the molecule, which is a fusion of a pyrazole ring and a pyrimidine ring. This structure is essential for its biological activity and interaction with various biological targets.
Functional Group
4-nitrophenyl group
Explanation: This refers to a phenyl ring attached to a nitro group (NO2) at the 4th position, which is known to influence the chemical behavior of the compound, including its reactivity and interaction with biological systems.
Potential Applications
Medicinal Chemistry
Explanation: The unique structure of 4H-Pyrazolo[3,4-d]pyrimidin-4-one, 1,5-dihydro-6-(4-nitrophenyl)- makes it a candidate for the development of small molecule inhibitors that can modulate biological processes. Its application in medicinal chemistry stems from its potential to interact with various enzymes and receptors, thereby affecting disease pathways.
Drug Design and Therapeutics
Scaffold for new drugs
Explanation: Its heterocyclic core and functional groups make it a valuable scaffold, or core structure, around which new drugs can be designed. This is crucial in the discovery and development of new therapeutic agents with improved efficacy and specificity.
Other Fields of Use
Materials Science, Organic Chemistry
Explanation: Beyond its potential in drug discovery and development, 4H-Pyrazolo[3,4-d]pyrimidin-4-one, 1,5-dihydro-6-(4-nitrophenyl)- may also find applications in materials science and organic chemistry, due to its unique chemical properties. This could include roles in the development of new materials or as a reagent in organic synthesis processes.
This list provides a comprehensive overview of the main properties and specific content related to 4H-Pyrazolo[3,4-d]pyrimidin-4-one, 1,5-dihydro-6-(4-nitrophenyl)-, illustrating its complex structure, potential applications, and significance in various scientific fields.
Check Digit Verification of cas no
The CAS Registry Mumber 21314-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,1 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 21314-14:
(7*2)+(6*1)+(5*3)+(4*1)+(3*4)+(2*1)+(1*4)=57
57 % 10 = 7
So 21314-14-7 is a valid CAS Registry Number.
21314-14-7Relevant academic research and scientific papers
Versatile synthesis of 6-alkyl/aryl-1H-pyrazolopyrimidin-4-ones
Reddy, K Hemender,Reddy, A Panduranga,Veeranagaiah, V
, p. 163 - 166 (2007/10/02)
Condensation of 5-amino-1H-pyrazole-4-carboxamide (1a) with various aromatic aldehydes furnishes 6-substituted-1H-pyrazolepyrimidin-4(5H)-ones (4a-f) via the intermediates 5-(N-arylideneamino)pyrazole-4-carboxamides (3a-f).Compounds 4a-f have also
