141122-62-5 Usage
Uses
Used in Chemical Synthesis:
3-HYDROXY-5-IODO (1H)INDAZOLE is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the development of new chemical entities.
Used in Pharmaceutical Research:
3-HYDROXY-5-IODO (1H)INDAZOLE is used as a starting material or building block in the design and synthesis of pharmaceutical compounds. The biological activities and therapeutic potential of indazole derivatives have been studied, and 3-HYDROXY-5-IODO (1H)INDAZOLE may contribute to the discovery of new drugs with improved efficacy and safety profiles.
Used in Medicinal Chemistry:
3-HYDROXY-5-IODO (1H)INDAZOLE is employed as a structural motif in the development of novel therapeutic agents. Its presence in a molecule can influence the pharmacokinetic and pharmacodynamic properties, potentially enhancing the drug's efficacy and selectivity for specific targets.
Used in Radiopharmaceuticals:
3-HYDROXY-5-IODO (1H)INDAZOLE, due to the presence of the iodine atom, can be used in the development of radiopharmaceuticals for diagnostic imaging. The iodine atom can be replaced with radioactive isotopes, allowing for the visualization of biological processes and the assessment of disease progression.
Used in Material Science:
3-HYDROXY-5-IODO (1H)INDAZOLE may also find applications in material science, where its unique structure and properties can be utilized to develop new materials with specific characteristics, such as conductivity, magnetism, or optical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 141122-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,1,2 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 141122-62:
(8*1)+(7*4)+(6*1)+(5*1)+(4*2)+(3*2)+(2*6)+(1*2)=75
75 % 10 = 5
So 141122-62-5 is a valid CAS Registry Number.
141122-62-5Relevant academic research and scientific papers
NEW CONVENIENT METHODS FOR THE SYNTHESIS OF 1,2-DIHYDRO-3H-INDAZOL-3-ONE AND ITS 1-ACYL DERIVATIVES
Dumitrascu, Florea,Plaveti, Marieta,Raileanu, Dan
, p. 917 - 924 (2007/10/03)
The acid hydrolysis of the readily obtainable 3-(o-carboxyphenyl)sydnones (6a-d) afforded 3-indazolones (3a-d) in yields over 90 percent. By transacylation between 1-acyl-3-acyloxyindazoles (11a-d) and 3-indazolones (3a, c), the corresponding 1-acyl-3-indazolones 10a-d resulted in pure state and yields also over 90 percent.