CAS 1072812-23-7: 7-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

Description: 7-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole is a chemical compound characterized by its indole core, which is a bicyclic structure containing a benzene ring fused to a pyrrole ring. The presence of a bromine atom at the 7-position enhances its reactivity and potential applications in organic synthesis and medicinal chemistry. The compound also features a boron-containing moiety, specifically a dioxaborolane, which is known for its utility in various chemical reactions, including Suzuki coupling reactions. The tetramethyl substitution on the dioxaborolane contributes to the compound's stability and steric hindrance, influencing its reactivity and solubility. This compound may be of interest in the development of pharmaceuticals or agrochemicals due to the unique properties imparted by both the indole and boron functionalities. Its specific applications would depend on further studies regarding its biological activity and reactivity in synthetic pathways.

Formula: C₁₄H₁₇BBrNO₂

InChI: InChI=1S/C14H17BBrNO2/c1-13(2)14(3,4)19-15(18-13)11-8-9-6-5-7-10(16)12(9)17-11/h5-8,17H,1-4H3

InChI key: InChIKey=KGWJGQUTNNLURY-UHFFFAOYSA-N

SMILES: BrC1=CC=CC=2C=C(NC12)B3OC(C)(C)C(O3)(C)C

7-BROMO-1H-INDOLE-2-BORONIC ACID PINACOL ESTER

CAS: 1072812-23-7

• Formula: C₁₄H₁₇BBrNO₂
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 322.0053

7-Bromoindole-2-boronic acid, pinacol ester

CAS: 1072812-23-7

• Molecular weight: 322.01g/mol

7-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

CAS: 1072812-23-7

• Purity: 95.0%
• Molecular weight: 322.010009765625

7-Bromoindole-2-boronic acid pinacol ester

CAS: 1072812-23-7

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• Formula: C₁₄H₁₇BBrNO₂
• Purity: Min. 95%
• Molecular weight: 322.01 g/mol