5-FLUOROPYRIDINE-2-BORONIC ACID
5-Fluoropyridine-2-boronic acid
CAS: 946002-10-4
Molecular Formula: C5H5BFNO2
5-FLUOROPYRIDINE-2-BORONIC ACID - Names and Identifiers
5-FLUOROPYRIDINE-2-BORONIC ACID - Physico-chemical Properties
| Molecular Formula | C5H5BFNO2 |
| Molar Mass | 140.908 |
| Density | 1.34 |
| Boling Point | 278.7℃ |
| Flash Point | 122.3℃ |
| pKa | 7.93±0.53(Predicted) |
| Storage Condition | Inert atmosphere,Store in freezer, under -20°C |
5-FLUOROPYRIDINE-2-BORONIC ACID - Introduction
5-Fluoropyridine-2-boronic acid is an organic compound with the chemical formula C5H5BFNO2. Its physical properties include a white to light yellow solid, a melting point of 105-110 degrees Celsius, and solubility in some polar solvents such as alcohols and ketones.
5-Fluoropyridine-2-boronic acid is mainly used as a boronating reagent in organic synthesis reactions. It can undergo nucleophilic reactions with other compounds to form chemical bonds. It is particularly suitable for Suzuki-Miyaura coupling reactions for the construction of carbon-carbon bonds. This reaction is very important for the design and preparation of synthetic natural products, drugs and organic molecules.
The preparation method of 5-Fluoropyridine-2-boronic acid can be achieved by reacting 5-Fluoropyridine-2-boronic acid ester with water or by reacting 5-Fluoropyridine-2-boronic acid sodium with acid.
Regarding safety information, 5-Fluoropyridine-2-boronic acid should be kept away from ignition sources and stored in a sealed container. Wear suitable personal protective equipment such as gloves and goggles during handling and use. It should not be in direct contact with the skin and eyes. Correct laboratory procedures should be followed during handling. If ingested or inhaled by mistake, seek medical attention immediately.
5-Fluoropyridine-2-boronic acid is mainly used as a boronating reagent in organic synthesis reactions. It can undergo nucleophilic reactions with other compounds to form chemical bonds. It is particularly suitable for Suzuki-Miyaura coupling reactions for the construction of carbon-carbon bonds. This reaction is very important for the design and preparation of synthetic natural products, drugs and organic molecules.
The preparation method of 5-Fluoropyridine-2-boronic acid can be achieved by reacting 5-Fluoropyridine-2-boronic acid ester with water or by reacting 5-Fluoropyridine-2-boronic acid sodium with acid.
Regarding safety information, 5-Fluoropyridine-2-boronic acid should be kept away from ignition sources and stored in a sealed container. Wear suitable personal protective equipment such as gloves and goggles during handling and use. It should not be in direct contact with the skin and eyes. Correct laboratory procedures should be followed during handling. If ingested or inhaled by mistake, seek medical attention immediately.
Last Update：2024-04-09 20:02:46
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Spot supply
Product Name: 5-Fluoropyridin-2-ylboronic acid Visit Supplier Webpage Request for quotationCAS: 946002-10-4
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328
WhatsApp: +86-18821248368
Product Name: 5-Fluoropyridine-2-boronic acid Visit Supplier Webpage Request for quotation
CAS: 946002-10-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
CAS: 946002-10-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
View History
5-FLUOROPYRIDINE-2-BORONIC ACID
[4-[(5-ethenyl-1-azabicyclo[2.2.2]oct-7-yl)-hydroxy-methyl]quinolin-6- yl] 3-methylbutanoate
3-Piperidinamine, N-[[2-methoxy-5-(1H-tetrazol-1-yl)phenyl]methyl]-2-phenyl-, (2R,3R)-
O-DesMethyl Venlafaxine DiMer
477320-16-4
2-Propenoic acid, 2-methyl-, C18-22-alkyl esters, C20-rich
(2,5-dichlorophenyl)(4-methylpiperazin-1-yl)methanone
2-methyl-N-(4-{[(4-methyl-2-pyrimidinyl)amino]sulfonyl}phenyl)propanamide
[4-[(5-ethenyl-1-azabicyclo[2.2.2]oct-7-yl)-hydroxy-methyl]quinolin-6- yl] 3-methylbutanoate
3-Piperidinamine, N-[[2-methoxy-5-(1H-tetrazol-1-yl)phenyl]methyl]-2-phenyl-, (2R,3R)-
O-DesMethyl Venlafaxine DiMer
477320-16-4
2-Propenoic acid, 2-methyl-, C18-22-alkyl esters, C20-rich
(2,5-dichlorophenyl)(4-methylpiperazin-1-yl)methanone
2-methyl-N-(4-{[(4-methyl-2-pyrimidinyl)amino]sulfonyl}phenyl)propanamide