329976-73-0
potassium benzyl(trifluoro)borate(1-)
CAS: 329976-73-0
Molecular Formula: C7H7BF3K
329976-73-0 - Names and Identifiers
| Name | potassium benzyl(trifluoro)borate(1-) |
| Synonyms | POTASSIUM BENZYLTRIFLUOROBORATE Potassium benzyltrifluoroborate BENZYLTRIFLUOROBORATE POTASSIUM SALT potassium benzyl(trifluoro)borate(1-) Potassium benzyl(trifluoro)borate(1-) |
| CAS | 329976-73-0 |
| InChI | InChI=1/C7H7BF3.K/c9-8(10,11)6-7-4-2-1-3-5-7;/h1-5H,6H2;/q-1;+1 |
| InChIKey | ANAJBFAVJLMYCY-UHFFFAOYSA-N |
329976-73-0 - Physico-chemical Properties
| Molecular Formula | C7H7BF3K |
| Molar Mass | 198.03 |
| Melting Point | >300 °C (lit.) |
| Storage Condition | Inert atmosphere,Room Temperature |
329976-73-0 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
| WGK Germany | 3 |
| HS Code | 29319090 |
329976-73-0 - Introduction
potassium benzyl(trifluoro)borate(1-) is an organic compound with the chemical formula C7H6BF3K. It has a colorless crystal or white powder, soluble in water and a variety of organic solvents.
The main use of this compound is as a reagent in organic synthesis, commonly used as a catalyst for benzylation reactions and other protonation reactions. It can promote electrophilic substitution reactions in organic molecules under appropriate reaction conditions, such as benzylation, acylation, etc.
The preparation method of potassium benzyl(trifluoro)borate(1-) is generally obtained by reacting benzyl sodium bromide with potassium trifluoroborate. First, sodium benzyl bromide and potassium trifluoroborate were dissolved in an organic solvent and reacted at an appropriate temperature to produce potassium borate(1-).
It is necessary to pay attention to its safety when using this compound. It may be irritating to the eyes, skin and respiratory tract, so wear protective equipment when handling this compound to avoid contact with skin and eyes. In addition, it should be operated in a well-ventilated place to avoid inhaling its vapors. In case of accidental exposure or discomfort, medical assistance should be sought immediately.
The main use of this compound is as a reagent in organic synthesis, commonly used as a catalyst for benzylation reactions and other protonation reactions. It can promote electrophilic substitution reactions in organic molecules under appropriate reaction conditions, such as benzylation, acylation, etc.
The preparation method of potassium benzyl(trifluoro)borate(1-) is generally obtained by reacting benzyl sodium bromide with potassium trifluoroborate. First, sodium benzyl bromide and potassium trifluoroborate were dissolved in an organic solvent and reacted at an appropriate temperature to produce potassium borate(1-).
It is necessary to pay attention to its safety when using this compound. It may be irritating to the eyes, skin and respiratory tract, so wear protective equipment when handling this compound to avoid contact with skin and eyes. In addition, it should be operated in a well-ventilated place to avoid inhaling its vapors. In case of accidental exposure or discomfort, medical assistance should be sought immediately.
Last Update：2024-04-10 22:29:15
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View History
329976-73-0
1257051-06-1
1271-94-9
82547-81-7
32018-96-5
6078-17-7
15217-42-2
16673-34-0
7414-83-7
2-(4-溴-3,5-二氟苯基)-2,2-二氟乙烷-1-醇
1257051-06-1
1271-94-9
82547-81-7
32018-96-5
6078-17-7
15217-42-2
16673-34-0
7414-83-7
2-(4-溴-3,5-二氟苯基)-2,2-二氟乙烷-1-醇