89466-08-0
89466-08-0
Chemical Structure
2-Hydroxyphenylboronic acid
- CAS No.: 89466-08-0
- Formula:C6H7BO3
- Molecular Weight:137.93
IUPAC Name: (2-hydroxyphenyl)boronic acid
InChIKey: YDMRDHQUQIVWBE-UHFFFAOYSA-N
SMILES: OB(C1=CC=CC=C1O)O
Biological Activity: 2-Hydroxyphenylboronic 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 | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
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. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Cyanophenylboronic acid | 99.93% | 2-Cyanophenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. 2-Cyanophenylboronic acid contains both nucleophilic and electrophilic centres. 2-Cyanophenylboronic acid can function as an efficient electrolyte additive for high voltage LCO cathode. 2-Cyanophenylboronic acid enhances the structural reversibililty and decreases the hydrofluoric acid formation. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
(2-Bromophenyl)boronic acid | 99.89% | (2-Bromophenyl)boronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Phenylboronic acid | 99.97% | Phenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Tolylboronic acid | 99.77% | 2-Tolylboronic acid is a biochemical analysis reagent and an important intermediate. 2-Tolylboronic acid can be used for the synthesis of other active compounds. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Fluorophenylboronic acid | 99.99% | 2-Fluorophenylboronic acid is an organic synthesis intermediate belonging to the fluorinated arylboronic acid class. The electron-withdrawing fluorine substituent in 2-Fluorophenylboronic acid reduces its pKa, thereby enhancing boronate bond formation with diols. 2-Fluorophenylboronic acid serves as a key synthetic intermediate for inhibitors of Plasmodium phosphatidylinositol 4-kinase IIIβ (PI4K). 2-Fluorophenylboronic acid can also be used to functionalize linear polyglycerols for constructing dual dynamic covalent cross-linked hydrogels that support 3D tumor spheroid culture of various cancer cells. 2-Fluorophenylboronic acid is applicable to research related to malaria and tumors. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
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 . | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Methoxyphenylboronic acid | 99.83% | 2-Methoxyphenylboronic acid is an arylboronic acid reagent and a Suzuki coupling substrate. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
(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. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
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. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Phenylboronic acid-13C6 | Phenylboronic acid-13C6 is the 13C-labeled Phenylboronic acid (HY-W001090). Phenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
