444010-34-8 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
1-(1-Adamantyl)-4-nitro-1H-pyrazole-3-carboxylic acid is used as a chemical intermediate for the synthesis of new drugs and bioactive molecules. Its unique structure and potential biological activity make it a valuable compound for exploring novel therapeutic properties and applications in the pharmaceutical industry.
Used in Chemical Synthesis:
In the chemical synthesis industry, 1-(1-Adamantyl)-4-nitro-1H-pyrazole-3-carboxylic acid is used as a key building block for the creation of more complex molecules with specific functions. Its rigid and metabolically stable nature allows for the development of compounds with tailored properties for various applications.
Used in Medicinal Chemistry:
1-(1-Adamantyl)-4-nitro-1H-pyrazole-3-carboxylic acid is utilized as a starting material in medicinal chemistry for the design and development of new pharmaceuticals. Its structural features can be exploited to target specific biological pathways or receptors, potentially leading to the discovery of innovative treatments for various diseases and conditions.
Used in Biochemical Research:
In the field of biochemical research, 1-(1-Adamantyl)-4-nitro-1H-pyrazole-3-carboxylic acid serves as a valuable tool for studying the interactions between small molecules and biological targets. Its unique structure can be used to probe the mechanisms of action of various enzymes, receptors, and other biomolecules, contributing to a deeper understanding of biological processes and the development of targeted therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 444010-34-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,0,1 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 444010-34:
(8*4)+(7*4)+(6*4)+(5*0)+(4*1)+(3*0)+(2*3)+(1*4)=98
98 % 10 = 8
So 444010-34-8 is a valid CAS Registry Number.
444010-34-8Relevant academic research and scientific papers
Adamantylazoles: IV acid-catalyzed adamantylation of pyrazoles
Gavrilov,Golod,Kachala,Ugrak
, p. 1741 - 1746 (2007/10/03)
Pyrazoles with pKBH+ no more than 0.8 and having substituents in 3(5) position with effective van der Waals radii not exceeding 2 A in a mixture of phosphoric and acetic acids at weight ratio 4 : 1 (H0 -1,8) react with 1-adamantanol to afford the corresponding 1-(1-adamantyl)-or 1,4-di(1-adamantyl)pyrazoles.
