CAS 1218791-00-4
:6-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
Description:
6-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 6-position of the indole enhances its reactivity and can facilitate various substitution reactions. The compound also features a boron-containing moiety, specifically a dioxaborolane, which is known for its utility in organic synthesis, particularly in cross-coupling reactions and as a boron source in various transformations. The tetramethyl substitution on the dioxaborolane contributes to the compound's stability and steric hindrance, influencing its reactivity. This compound may be of interest in medicinal chemistry and materials science due to its potential applications in drug development and as a building block in organic synthesis. Its unique structural features make it a valuable candidate for further research in various chemical applications.
Formula:C14H17BBrNO2
InChI:InChI=1S/C14H17BBrNO2/c1-13(2)14(3,4)19-15(18-13)12-7-9-5-6-10(16)8-11(9)17-12/h5-8,17H,1-4H3
InChI key:InChIKey=BTDQQZKRCOKCTM-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC=3C(N2)=CC(Br)=CC3
Synonyms:- 1H-Indole, 6-bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
- 6-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
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Found 4 products.
6-bromoindole-2-boronic acid pinacol ester
CAS:Formula:C14H17BBrNO2Purity:98%Color and Shape:SolidMolecular weight:322.00536-Bromoindole-2-boronic acid, pinacol ester
CAS:6-Bromoindole-2-boronic acid, pinacol esterPurity:98%Molecular weight:322.01g/mol6-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
CAS:Purity:98%Molecular weight:322.01000986-Bromoindole-2-boronic acid pinacol ester
CAS:<p>Versatile small molecule scaffold</p>Formula:C14H17BBrNO2Purity:Min. 95%Molecular weight:322.01 g/mol



