CAS 837392-56-0
:7-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
Description:
7-Fluoro-5-(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 consisting of a benzene ring fused to a pyrrole ring. The presence of a fluorine atom at the 7-position enhances its electronic properties, potentially influencing its reactivity and biological activity. 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 in organic synthesis. The tetramethyl substitution on the boron compound provides steric hindrance, which can affect the compound's solubility and reactivity. Overall, this compound may exhibit interesting properties for applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the combination of its indole structure and boron functionality. Its unique characteristics make it a subject of interest for further research in synthetic and medicinal chemistry.
Formula:C14H17BFNO2
InChI:InChI=1S/C14H17BFNO2/c1-13(2)14(3,4)19-15(18-13)10-7-9-5-6-17-12(9)11(16)8-10/h5-8,17H,1-4H3
InChI key:InChIKey=UYRCCVKIZZPVAY-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C=C3C(=C(F)C2)NC=C3
Synonyms:- 7-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
- 1H-Indole, 7-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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Found 3 products.
7-Fluoro-1H-indole-5-boronic acid, pinacol ester
CAS:<p>7-Fluoro-1H-indole-5-boronic acid, pinacol ester</p>Purity:≥95%Color and Shape:SolidMolecular weight:261.10g/mol7-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
CAS:Purity:98+%Molecular weight:261.1000061


