7364-26-3 Usage
Uses
Used in Organic Synthesis:
3-HYDROXY-5-METHYL (1H)INDAZOLE is used as a building block for the synthesis of various organic compounds, contributing to the development of new chemical entities and materials.
Used in Medicinal Chemistry:
3-HYDROXY-5-METHYL (1H)INDAZOLE is used as a key intermediate in the design and synthesis of pharmaceuticals, due to its potential pharmacological properties and its role in drug development.
Used in Pharmaceutical Research and Development:
3-HYDROXY-5-METHYL (1H)INDAZOLE is used as a compound of interest in the discovery and development of new drugs, particularly in the areas of antimicrobial and anti-cancer therapies.
Used in Antimicrobial Applications:
3-HYDROXY-5-METHYL (1H)INDAZOLE is used as an antimicrobial agent, potentially effective against various types of bacteria and other microorganisms, contributing to the development of new treatments for infectious diseases.
Used in Anti-Cancer Applications:
3-HYDROXY-5-METHYL (1H)INDAZOLE is used as an anti-cancer agent, being studied for its potential to inhibit the growth and proliferation of cancer cells, and to contribute to the development of novel cancer therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 7364-26-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,6 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7364-26:
(6*7)+(5*3)+(4*6)+(3*4)+(2*2)+(1*6)=103
103 % 10 = 3
So 7364-26-3 is a valid CAS Registry Number.
7364-26-3Relevant academic research and scientific papers
Johnson, Barry L.,Rodgers, James D.
, p. 2681 - 2684 (2005)
A clean, high-yielding synthetic route to methyl 5-(bromomethyl)-1- tritylindazole 3-carboxylate 1 was needed. A principal intermediate was 5-methyl-3-carboxyindazole 2. An analysis of a by-product found after executing Schad's 3-carboxyindazole synthesis led to undertaking this reaction with an inverse addition in the principal step. This simple modification gave 2 in excellent and reproducible yields. Copyright Taylor & Francis, Inc.
