87199-18-6
87199-18-6
Chemical Structure
(3-Hydroxyphenyl)boronic acid
Synonym(s): 3-Hydroxybenzeneboronic acid
- CAS No.: 87199-18-6
- Formula:C6H7BO3
- Molecular Weight:137.93
IUPAC Name: (3-hydroxyphenyl)boronic acid
InChIKey: WFWQWTPAPNEOFE-UHFFFAOYSA-N
SMILES: OB(C1=CC=CC(O)=C1)O
Biological Activity: (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[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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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-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-Methoxybenzeneboronic acid | 99.95% | 3-Methoxybenzeneboronic acid (3-Methoxyphenylboronic acid) is a boronic acid derivative. 3-Methoxybenzeneboronic acid shows best suitable binding pattern at the active site by interacting non-covalently with amino acid residues of proteins. 3-Methoxybenzeneboronic 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 monohydrate | 99.50% | 3-Aminophenylboronic acid monohydrate is a phenylboronic acid derivative. 3-Aminophenylboronic acid monohydrate 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-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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2-Hydroxyphenylboronic acid | 99.11% | 2-Hydroxyphenylboronic 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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6-Hydroxypyridin-3-ylboronic acid | 6-Hydroxypyridin-3-ylboronic acid is a heterocyclic building block, which can be used in the synthesis of non-nucleoside inhibitors of hepatitis C virus (HCV) RNA-dependent RNA polymerase nonstructural protein 5B (NS5B). 6-Hydroxypyridin-3-ylboronic acid has also been used in the synthesis of mammalian target of rapamycin (mTOR) 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-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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