CymitQuimica logo

CAS 1256360-06-1

:

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

Description:
Ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1-carboxylate is a chemical compound characterized by its unique structure, which includes a pyrrole ring and a dioxaborolane moiety. The presence of the ethyl ester group contributes to its solubility in organic solvents, making it suitable for various synthetic applications. The dioxaborolane group is known for its utility in organic synthesis, particularly in the formation of boron-containing compounds, which can participate in cross-coupling reactions. This compound may exhibit interesting reactivity due to the electron-rich nature of the pyrrole ring, potentially allowing for electrophilic substitution reactions. Additionally, the bulky tetramethyl groups in the dioxaborolane can influence steric hindrance and reactivity. Overall, this compound is of interest in the fields of organic chemistry and materials science, particularly in the development of new synthetic methodologies and functional materials. Its specific properties, such as melting point, boiling point, and reactivity, would require experimental determination for precise applications.
Formula:C13H20BNO4
InChI:InChI=1S/C13H20BNO4/c1-6-17-11(16)15-8-7-10(9-15)14-18-12(2,3)13(4,5)19-14/h7-9H,6H2,1-5H3
InChI key:InChIKey=DYCDAHNPZKXBBH-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CN(C(OCC)=O)C=C2
Synonyms:
  • Ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1-carboxylate
  • 1H-Pyrrole-1-carboxylic acid, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, ethyl ester
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.