CymitQuimica logo

CAS 1256360-11-8

:

Phenylmethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1-carboxylate

Description:
Phenylmethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1-carboxylate is a chemical compound characterized by its complex structure, which includes a pyrrole ring and a boron-containing moiety. The presence of the tetramethyl-1,3,2-dioxaborolane group suggests that this compound may exhibit unique reactivity, particularly in cross-coupling reactions, making it potentially useful in organic synthesis and medicinal chemistry. The pyrrole ring contributes to the compound's aromaticity and may influence its electronic properties, while the ester functional group (carboxylate) can participate in various chemical reactions, including hydrolysis and transesterification. This compound may also exhibit specific solubility characteristics depending on the solvent used, and its stability can be influenced by environmental factors such as temperature and light. Overall, the combination of these functional groups suggests that this compound could have applications in the development of pharmaceuticals or advanced materials, although specific applications would depend on further research and characterization.
Formula:C18H22BNO4
InChI:InChI=1S/C18H22BNO4/c1-17(2)18(3,4)24-19(23-17)15-10-11-20(12-15)16(21)22-13-14-8-6-5-7-9-14/h5-12H,13H2,1-4H3
InChI key:InChIKey=MHUYEVSKFAMONG-UHFFFAOYSA-N
SMILES:C(OCC1=CC=CC=C1)(=O)N2C=C(C=C2)B3OC(C)(C)C(C)(C)O3
Synonyms:
  • 1H-Pyrrole-1-carboxylic acid, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, phenylmethyl ester
  • Phenylmethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1-carboxylate
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.