150255-96-2
150255-96-2
Chemical Structure
3-Cyanophenylboronic acid
- CAS No.: 150255-96-2
- Formula:C7H6BNO2
- Molecular Weight:146.94
IUPAC Name: (3-cyanophenyl)boronic acid
InChIKey: XDBHWPLGGBLUHH-UHFFFAOYSA-N
SMILES: N#CC1=CC(B(O)O)=CC=C1
Biological Activity: 3-Cyanophenylboronic acid is an arylboronic acid-based boronic acid reagent that serves as a coupling partner in Suzuki-Miyaura cross-coupling reactions. 3-Cyanophenylboronic acid participates in reactions to synthesize 4'-propoxybiphenyl-3-carbonitrile[1][2].
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3-Cyanophenylboronic acid | 99.42% | 3-Cyanophenylboronic acid is an arylboronic acid-based boronic acid reagent that serves as a coupling partner in Suzuki-Miyaura cross-coupling reactions. 3-Cyanophenylboronic acid participates in reactions to synthesize 4'-propoxybiphenyl-3-carbonitrile. | ||||||||||||||||||||
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References
- [1]. Cárdenas-Valenzuela A J, et al. Crystal structure and Hirshfeld surface analysis of 3-cyanophenylboronic acid[J]. Structure Reports, 2018, 74(4): 441-444.
- [2]. Bang JS, et al. Small molecules that regulate zymosan phagocytosis of macrophage through deactivation of Rho GTPases. Bioorganic & medicinal chemistry. 2012 Sep 01;20(17):5262-8.
Keywords
