CAS 864770-82-1
:1-N-Boc-3-Methylindazole-5-boronicacidpinacolester
Description:
1-N-Boc-3-Methylindazole-5-boronic acid pinacol ester, identified by its CAS number 864770-82-1, is a boronic acid derivative that features a boron atom bonded to a pinacol ester and an indazole moiety. The "Boc" (tert-butoxycarbonyl) group serves as a protecting group for the amine, enhancing the compound's stability and solubility in organic solvents. This compound is characterized by its ability to participate in Suzuki coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The presence of the methyl group at the 3-position of the indazole ring can influence its reactivity and sterics, while the boronic acid functionality allows for further derivatization. Typically, such compounds are utilized in medicinal chemistry and materials science for the development of pharmaceuticals and advanced materials. Its physical properties, such as solubility and melting point, would depend on the specific conditions and purity of the compound.
Formula:C19H27BN2O4
InChI:InChI=1S/C19H27BN2O4/c1-12-14-11-13(20-25-18(5,6)19(7,8)26-20)9-10-15(14)22(21-12)16(23)24-17(2,3)4/h9-11H,1-8H3
SMILES:Cc1c2cc(ccc2n(C(=O)OC(C)(C)C)n1)B1OC(C)(C)C(C)(C)O1
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Found 3 products.
1-N-Boc-3-methyl-indazole-5-boronic acid pinacol ester
CAS:Formula:C19H27BN2O4Purity:97%Color and Shape:SolidMolecular weight:358.23971-N-BOC-3-methyl-indazole-5-boronic acid, pinacol ester
CAS:<p>1-N-BOC-3-methyl-indazole-5-boronic acid, pinacol ester</p>Purity:97%Molecular weight:358.24g/moltert-Butyl 3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole-1-carboxylate
CAS:Purity:97%Molecular weight:358.25


