163105-89-3
163105-89-3
Chemical Structure
2-Methoxypyridine-5-boronic acid
- CAS No.: 163105-89-3
- Formula:C6H8BNO3
- Molecular Weight:152.94
IUPAC Name: (6-methoxypyridin-3-yl)boronic acid
InChIKey: DHADXDMPEUWEAS-UHFFFAOYSA-N
SMILES: COC1=CC=C(B(O)O)C=N1
Biological Activity: 2-Methoxypyridine-5-boronic 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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2-Methoxypyridine-5-boronic acid | 99.84% | 2-Methoxypyridine-5-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-Fluoro-4-methoxyphenyl)boronic acid | 99.99% | (3-Fluoro-4-methoxyphenyl)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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2-Fluoropyridine-5-boronic acid | 99.95% | 2-Fluoropyridine-5-boronic acid (6-Fluoropyridine-3-boronic acid) is a fatty acid amide hydrolase (FAAH) inhibitor with an IC50 of 10 μM. 2-Fluoropyridine-5-boronic acid is applicable to research related to inflammation and pain. | ||||||||||||||||||||
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2-Chloropyridine-5-boronic acid | 99.77% | 2-Chloropyridine-5-boronic acid is a mandelate racemase (MR) inhibitor with a Ki value of 8.5 μM against Pseudomonas putida MR. | ||||||||||||||||||||
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2-Methoxypyridine-3-boronic acid | 98.0% | 2-Methoxypyridine-3-boronic acid is a pyridine boronic acid compound and also borylation reagent used in Suzuki cross-coupling reactions. | ||||||||||||||||||||
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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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4-Methoxyphenylboronic acid | 99.83% | 4-Methoxyphenylboronic 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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(2-Methoxypyrimidin-5-yl)boronic acid | 99.86% | (2-Methoxypyrimidin-5-yl)boronic acid is a drug intermediate that can serve as a key reactant in the Suzuki-Miyaura coupling reaction, and is used for the synthesis of isoquinoline ketone derivatives with anti-tumor activity. | ||||||||||||||||||||
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6-Aminopyridine-3-boronic acid | 6-Aminopyridine-3-boronic acid is a boronic acid derivative. Boronic acid derivatives are widely used in organic synthesis for carbon-carbon bond formation. In Suzuki coupling, aryl halides and boronic acid aryl or vinyl esters or boronic acid are coupled using Pd(PPh3)4. It can be used as a pharmaceutical intermediate. | |||||||||||||||||||||
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BPBA | 99.85% | BPBA (2-Bromopyridine-5-boronic acid) is a derivatization reagent derived from Boric acid (HY-Y0314) with enhanced ionization efficiency in positive-mode electrospray ionization mass spectrometry. BPBA forms boronate ester derivatives with vicinal diols. It enables rapid, catalyst-free labeling operations, improves the detection sensitivity of liquid chromatography/mass spectrometry, and reduces false positive errors. | ||||||||||||||||||||
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