63503-60-6
Chemical Structure
3-Chlorophenyl boronic acid
- CAS No.: 63503-60-6
- Formula:C6H6BClO2
- Molecular Weight:156.38
IUPAC Name: 3-chlorophenyl boronic acid
InChIKey: SDEAGACSNFSZCU-UHFFFAOYSA-N
SMILES: ClC1=CC=CC(B(O)O)=C1
Biological Activity: 3-Chlorophenylboronic acid is employed as a reactant involved in 1,4-conjugate addition reactions with ethenesulfonamides to form arylethanesulfonamides, Suzuki-Miyaura reactions with dibromotrifluoromethylbenzene, cross-coupling reactions with diazoesters3 or potassium cyanate. 3-Chlorophenylboronic acid is involved in the synthesis of biarylketones and phthalides and synthesis of inhibitors including PDE4 inhibitors among others. 3-Chlorophenyl boronic acid can affect cell migration. 3-Chlorophenyl boronic acid can be used to study wound healing [1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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3-Chlorophenyl boronic acid | 99.88% | 3-Chlorophenylboronic acid is employed as a reactant involved in 1,4-conjugate addition reactions with ethenesulfonamides to form arylethanesulfonamides, Suzuki-Miyaura reactions with dibromotrifluoromethylbenzene, cross-coupling reactions with diazoesters3 or potassium cyanate. 3-Chlorophenylboronic acid is involved in the synthesis of biarylketones and phthalides and synthesis of inhibitors including PDE4 inhibitors among others. 3-Chlorophenyl boronic acid can affect cell migration. 3-Chlorophenyl boronic acid can be used to study wound healing . | ||||||||||||||||||||
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Keywords
