5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-Pyridinamine
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-pyridinamine
CAS: 944401-57-4
Molecular Formula: C12H16BF3N2O2
5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-Pyridinamine - Names and Identifiers
5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-Pyridinamine - Physico-chemical Properties
| Molecular Formula | C12H16BF3N2O2 |
| Molar Mass | 288.07 |
| Density | 1.23 |
| Boling Point | 375.0±42.0 °C(Predicted) |
| Water Solubility | Slightly soluble in water. |
| pKa | 4.83±0.37(Predicted) |
| Storage Condition | 2-8°C(protect from light) |
| MDL | MFCD12923420 |
5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-Pyridinamine - Introduction
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-pyridinamine is an organic compound with the chemical formula C11H13BF3N2O2.
Nature:
-Appearance: 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-pyridinamine is a white to yellowish solid.
-Melting point: about 140-144°C.
-Solubility: Good solubility in common organic solvents such as ethanol, dimethyl sulfoxide and dichloromethane.
Use:
- 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-pyridinamine is an important organic boron reagent, which can be used in various chemical reactions, such as Suzuki coupling reaction, Stille coupling reaction and Sonogashira coupling reaction.
-It can also be used for catalytic reactions in organic synthesis and the synthesis of functional materials.
Method:
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-pyridinamine is usually structurally identified by nuclear magnetic resonance spectroscopy (NMR), infrared spectroscopy (IR) and other techniques. The preparation generally involves carrying out a substitution reaction on pyridine, followed by reaction with a trifluoromethyl borate to give the target compound.
Safety Information:
Safety information on 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-pyridinamine is currently limited, so it needs to be used, stored and handled under reasonable protective conditions.
Nature:
-Appearance: 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-pyridinamine is a white to yellowish solid.
-Melting point: about 140-144°C.
-Solubility: Good solubility in common organic solvents such as ethanol, dimethyl sulfoxide and dichloromethane.
Use:
- 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-pyridinamine is an important organic boron reagent, which can be used in various chemical reactions, such as Suzuki coupling reaction, Stille coupling reaction and Sonogashira coupling reaction.
-It can also be used for catalytic reactions in organic synthesis and the synthesis of functional materials.
Method:
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-pyridinamine is usually structurally identified by nuclear magnetic resonance spectroscopy (NMR), infrared spectroscopy (IR) and other techniques. The preparation generally involves carrying out a substitution reaction on pyridine, followed by reaction with a trifluoromethyl borate to give the target compound.
Safety Information:
Safety information on 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-2-pyridinamine is currently limited, so it needs to be used, stored and handled under reasonable protective conditions.
Last Update：2024-04-10 22:29:15
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Product Name: 2-Amino-4-(trifluoromethyl)pyridine-5-boronic acid pinacol ester Visit Supplier Webpage Request for quotation
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