CAS NO:459133-68-7 1-Boc-5-Bromo-3-Iodo-1H-Indazole
CAS NO:459133-68-7 NAME:1-Boc-5-Bromo-3-Iodo-1H-Indazole MF：C12H12BrIN2O2 MW：423.04 PURITY:95%MIN FP:222℃ COA:Available
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Material Chemistry
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Product introduction
| PRODUCT NAME | 1-Boc-5-Bromo-3-Iodo-1H-Indazole |
| CAS NO | 459133-68-7 |
| APPEARANCE | ASKED |
| BP | 444℃ |
| DENSITY | 1.91 |
| STORAGE | 2-8°C |
| DELIVERY | 2-3DAYS |
| PACKAGE | Keep in dark place,Sealed in dry,Room Temperature |
Description of CAS NO:459133-68-7 1-Boc-5-Bromo-3-Iodo-1H-Indazole
other name :
3-IODO-5-BROMO-1H-INDAZOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
tert-butyl 5-bromo-3-iodo-1H-indazole-1-carboxylate
It is used in various chemical reactions and has a molecular weight of 423.04 g/mol
Applications of CAS NO:459133-68-7 1-Boc-5-Bromo-3-Iodo-1H-Indazole
1)Click Chemistry in Drug Discovery;
2)Ruthenium-Catalyzed Synthesis for Triazole Scaffolds
The ruthenium-catalyzed cycloaddition process allows for the preparation of triazole-based scaffolds, a significant structure in medicinal chemistry. This methodology enables the synthesis of peptidomimetics or biologically active compounds, demonstrating the versatility and importance of indazole derivatives in creating molecules with potential therapeutic applications;
3)Development of Novel Indazole Derivatives
Indazoles are subjected to various synthetic manipulations to generate novel derivatives with potential biological activities;
4)Supramolecular Interactions of Triazoles
Beyond their synthetic accessibility, 1,2,3-triazoles, closely related to indazole derivatives, exhibit a unique combination of facile synthesis and diverse supramolecular interactions. These properties make them suitable for applications in supramolecular chemistry, coordination chemistry, anion recognition, catalysis, and photochemistry.
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