135884-31-0
Chemical Structure
N-Boc-2-pyrroleboronic acid
- CAS No.: 135884-31-0
- Formula:C9H14BNO4
- Molecular Weight:211.03
IUPAC Name: (1-(tert-butoxycarbonyl)-1H-pyrrol-2-yl)boronic acid
InChIKey: ZWGMJLNXIVRFRJ-UHFFFAOYSA-N
SMILES: O=C(N1C(B(O)O)=CC=C1)OC(C)(C)C
Biological Activity: N-Boc-2-pyrroleboronic acid is an organic synthesis intermediate used primarily in the synthesis of chiral pharmaceutical molecules and biologically active molecules. The boronic acid on the pyrrole ring can participate in Suzuki coupling reactions. The boronic acid can be oxidized to a hydroxyl group under the action of nitrogen oxides, and after tautomerization, it can be further transformed into 2-oxo-2,5-dihydro-1-pyrrolecarboxylic acid tert-butyl ester[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
N-Boc-2-pyrroleboronic acid | 99.65% | N-Boc-2-pyrroleboronic acid is an organic synthesis intermediate used primarily in the synthesis of chiral pharmaceutical molecules and biologically active molecules. The boronic acid on the pyrrole ring can participate in Suzuki coupling reactions. The boronic acid can be oxidized to a hydroxyl group under the action of nitrogen oxides, and after tautomerization, it can be further transformed into 2-oxo-2,5-dihydro-1-pyrrolecarboxylic acid tert-butyl ester. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
Keywords
