87199-16-4
87199-16-4
Chemical Structure
3-Formylphenylboronic acid
- CAS No.: 87199-16-4
- Formula:C7H7BO3
- Molecular Weight:149.94
IUPAC Name: (3-formylphenyl)boronic acid
InChIKey: HJBGZJMKTOMQRR-UHFFFAOYSA-N
SMILES: OB(C1=CC=CC(C=O)=C1)O
Biological Activity: 3-Formylphenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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3-Formylphenylboronic acid | 98.04% | 3-Formylphenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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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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(3-Fluoro-2-formylphenyl)boronic acid | (3-Fluoro-2-formylphenyl)boronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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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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(3-Hydroxyphenyl)boronic acid | 99.90% | (3-Hydroxyphenyl)boronic acid (3-Hydroxybenzeneboronic acid) is a drug intermediate that can be used for the synthesis of 17β-hydroxysteroid dehydrogenase type 1 inhibitors. | ||||||||||||||||||||
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3-Bromophenylboronic acid | 98.0% | 3-Bromophenylboronic acid is an arylboronic acid reagent that can be used as a Suzuki coupling substrate. | ||||||||||||||||||||
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3-Tolylboronic acid | 98.0% | 3-Tolylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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(3-Hydroxymethyl)phenylboronic acid | 98.27% | 3-(Hydroxymethyl)phenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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3-Fluoro-4-formylphenylboronic acid | 99.48% | 3-Fluoro-4-formylphenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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3-Aminophenylboronic acid | 99.93% | 3-Aminophenylboronic acid (m-Aminophenylboronic acid) is a phenylboronic acid derivative. 3-Aminophenylboronic acid reacts covalently with cis-diol groups of glycoproteins, enabling selective capture and detection of glycoproteins through fluorescence quenching of APBA-functionalized copper nanoclusters. | ||||||||||||||||||||
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3-Carboxyphenylboronic acid | 99.97% | 3-Carboxyphenylboronic acid is a biochemical reagent with multiple functions including nanoparticle enhancement, perovskite passivation, fluorescence quenching, and adhesion. 3-Carboxyphenylboronic acid improves tumor penetration and pulmonary retention of nanoparticles, and serves as a tumor-targeting ligand for carboxymethyl chitosan nanoparticles. 3-Carboxyphenylboronic acid optimizes film crystallization via coordinate chelation of free lead/iodide ions in perovskites. 3-Carboxyphenylboronic acid acts as an additive for n-i-p perovskite solar cells. Conjugation of 3-Carboxyphenylboronic acid with PPEG8 quenches the near-infrared fluorescence of single-walled carbon nanotubes, enabling aqueous dispersion of carbon nanotubes through binding to the diol structure of saccharides. | ||||||||||||||||||||
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