1-BOC-7-Chloroindole-3-boronic acid, pinacol ester

• CAT Number: M032411
• CAS Number: 1218790-31-8
• Molecular Formula: C19H25BClNO4
• Molecular Weight: 377.67
• Purity: ≥95%
• Storage: Store at +4C
• IUPAC Name: tert-butyl 7-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indole-1-carboxylate
• InChI: InChI=1S/C19H25BClNO4/c1-17(2,3)24-16(23)22-11-13(12-9-8-10-14(21)15(12)22)20-25-18(4,5)19(6,7)26-20/h8-11H,1-7H3
• InChIKey: BEBXOCOXQGXHIB-UHFFFAOYSA-N
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CN(C3=C2C=CC=C3Cl)C(=O)OC(C)(C)C

1-BOC-7-Chloroindole-3-boronic acid, pinacol ester(CAT: M032411) is a high-purity boronic ester widely used in pharmaceutical and chemical research. Featuring a 7-chloroindole core protected by a tert-butoxycarbonyl (BOC) group, this compound is functionalized with a boronic acid pinacol ester at the 3-position, making it a versatile intermediate for Suzuki-Miyaura cross-coupling reactions. Its unique structure supports the synthesis of complex bioactive molecules, including drug candidates and advanced materials. 1-BOC-7-Chloroindole-3-boronic acid, pinacol ester ensures consistent reactivity and performance, facilitating innovation in medicinal chemistry, organic synthesis, and material science applications.