885523-89-7 Usage
Uses
Used in Medicinal Chemistry:
6-Bromo-3-iodo-4-(1H)indazole methyl carboxylate is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique molecular structure and pharmacological properties make it a promising candidate for the development of new therapeutic agents.
Used in Drug Discovery:
6-Bromo-3-iodo-4-(1H)indazole methyl carboxylate is used as a lead compound in drug discovery. Its potential biological activities and interactions with target proteins can be explored to identify novel therapeutic agents for various diseases.
Used in Synthesis of Bioactive Molecules:
6-Bromo-3-iodo-4-(1H)indazole methyl carboxylate is used as a key building block in the synthesis of bioactive molecules. Its chemical reactivity and structural features can be exploited to create new compounds with potential therapeutic applications.
Used in Research and Development:
6-Bromo-3-iodo-4-(1H)indazole methyl carboxylate is used as a research tool in the field of medicinal chemistry. It can be employed to study the structure-activity relationships of indazole derivatives and to investigate their potential as therapeutic agents.
Used in Pharmaceutical Industry:
6-Bromo-3-iodo-4-(1H)indazole methyl carboxylate is used as a raw material in the pharmaceutical industry for the production of drugs. Its unique properties and potential applications make it a valuable component in the development of new medications.
Check Digit Verification of cas no
The CAS Registry Mumber 885523-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,5,2 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 885523-89:
(8*8)+(7*8)+(6*5)+(5*5)+(4*2)+(3*3)+(2*8)+(1*9)=217
217 % 10 = 7
So 885523-89-7 is a valid CAS Registry Number.
885523-89-7Relevant academic research and scientific papers
Zhang, Jiawei,Kong, Kaimin,Li, Xiangjun,Zhang, Qian
, p. 2365 - 2376 (2021)
An intriguing ring-opening reaction of 1-arylsulfonyl-3-iodo-1H-indazoles, which can afford the corresponding ortho-(arylsulfonylamino)benzonitriles under base catalysis, was obtained unexpectedly. Herein, the optimal reaction conditions were explored and
