CymitQuimica logo

CAS 1256360-12-9

:

Phenyl[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrol-1-yl]methanone

Description:
Phenyl[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrol-1-yl]methanone, with the CAS number 1256360-12-9, is a chemical compound characterized by its complex structure, which includes a phenyl group, a pyrrole ring, and a dioxaborolane moiety. This compound is likely to exhibit properties typical of organic compounds containing boron, such as potential reactivity in cross-coupling reactions, making it of interest in organic synthesis and materials science. The presence of the dioxaborolane group suggests it may participate in boron-mediated reactions, which are valuable in the formation of carbon-carbon bonds. Additionally, the pyrrole ring contributes to the compound's aromaticity and may influence its electronic properties. The tetramethyl substitution on the dioxaborolane enhances its steric bulk, potentially affecting its solubility and reactivity. Overall, this compound may find applications in medicinal chemistry, agrochemicals, or as a building block in the synthesis of more complex molecules.
Formula:C17H20BNO3
InChI:InChI=1S/C17H20BNO3/c1-16(2)17(3,4)22-18(21-16)14-10-11-19(12-14)15(20)13-8-6-5-7-9-13/h5-12H,1-4H3
InChI key:InChIKey=ODVABAFGSMXFEL-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CN(C(=O)C3=CC=CC=C3)C=C2
Synonyms:
  • Phenyl[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrol-1-yl]methanone
  • Methanone, phenyl[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrol-1-yl]-
Sort by

Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.