CAS 1086391-06-1
:Methyl 3-bromo-1H-indazole-5-carboxylate
Description:
Methyl 3-bromo-1H-indazole-5-carboxylate is a chemical compound characterized by its indazole core, which is a bicyclic structure containing a five-membered ring fused to a six-membered ring. The presence of a bromine atom at the 3-position and a carboxylate group at the 5-position contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. The methyl ester functional group enhances its solubility in organic solvents, making it suitable for various chemical reactions. This compound may exhibit biological activity, which is often explored in drug discovery and development. Its molecular structure allows for potential interactions with biological targets, making it of interest in pharmacological studies. Additionally, the presence of halogen substituents like bromine can influence the compound's electronic properties and reactivity, potentially leading to unique chemical behavior. Overall, Methyl 3-bromo-1H-indazole-5-carboxylate is a versatile compound with significant implications in research and development within the fields of chemistry and biochemistry.
Formula:C9H7BrN2O2
InChI:InChI=1S/C9H7BrN2O2/c1-14-9(13)5-3-2-4-6-7(5)8(10)12-11-6/h2-4H,1H3,(H,11,12)
SMILES:COC(=O)c1cccc2c1c(Br)n[nH]2
Synonyms:- 1H-Indazole-5-carboxylic acid, 3-bromo-, methyl ester
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Found 4 products.
Methyl 3-bromo-1H-indazole-5-carboxylate
CAS:Formula:C9H7BrN2O2Purity:98%Color and Shape:SolidMolecular weight:255.0681Methyl 3-bromo-1H-indazole-5-carboxylate
CAS:<p>Methyl 3-bromo-1H-indazole-5-carboxylate</p>Purity:99%Molecular weight:255.07g/molMethyl 3-bromo-1H-indazole-5-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H7BrN2O2Purity:Min. 95%Molecular weight:255.07 g/mol



