458532-96-2
458532-96-2
Chemical Structure
2-Chloropyridine-4-boronic acid
- CAS No.: 458532-96-2
- Formula:C5H5BClNO2
- Molecular Weight:157.37
IUPAC Name: (2-chloropyridin-4-yl)boronic acid
InChIKey: WJYRVVDXJMJLTN-UHFFFAOYSA-N
SMILES: ClC1=NC=CC(B(O)O)=C1
Biological Activity: 2-Chloropyridine-4-boronic acid is an intermediate. 2-Chloropyridine-4-boronic acid can be used in the synthesis of nAChR agonists. 2-Chloropyridine-4-boronic acid can be used in cancer research[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2-Chloropyridine-4-boronic acid | 98.25% | 2-Chloropyridine-4-boronic acid is an intermediate. 2-Chloropyridine-4-boronic acid can be used in the synthesis of nAChR agonists. 2-Chloropyridine-4-boronic acid can be used in cancer research. | ||||||||||||||||||||
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3,4-Dichlorophenylboronic acid | 3,4-Dichlorophenylboronic 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-Chloro-3-fluorophenylboronic acid | 4-Chloro-3-fluorophenylboronic 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-4-boronic acid | 99.78% | 2-Fluoropyridine-4-boronic acid is a coupling reagent and chemical intermediate. 2-Fluoropyridine-4-boronic acid facilitates the synthesis of Rho kinase (ROCK) inhibitor Compound 37. | ||||||||||||||||||||
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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-3-boronic acid | 2-Chloropyridine-3-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-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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3-Chloro-4-fluorophenylboronic acid | 3-Chloro-4-fluorophenylboronic 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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(2,6-Dichloropyridin-4-yl)boronic acid | 99.93% | (2,6-Dichloropyridin-4-yl)boronic acid is a chemical catalyst used in biochemical reactions. | ||||||||||||||||||||
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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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