(3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid
(3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid
CAS: 1256346-02-7
Molecular Formula: C10H12BF3O4
(3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid - Names and Identifiers
(3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid - Physico-chemical Properties
| Molecular Formula | C10H12BF3O4 |
| Molar Mass | 264.01 |
| Density | 1.31±0.1 g/cm3(Predicted) |
| Boling Point | 348.3±52.0 °C(Predicted) |
| pKa | 6.99±0.10(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD16618933 |
(3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid - Introduction
(3-Propoxy-5-(trifluoromethoxy)phenyl)boronic is an organoboron compound with the chemical formula C12H14BF3O4. It is a solid with certain solubility and can be dissolved in common organic solvents. The compound is an intermediate of a dehydration condensation reaction.
(3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid has a wide range of applications in chemical research and organic synthesis. It can be used in the synthesis of boron-containing organic compounds, such as anionic borate esters. These compounds have important applications in drug discovery and ligand design, for example, they act as inhibitors of Tyr-Kinase enzyme activity. In addition,(3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid can also be used as an organic material for optoelectronic devices.
One method for preparing (3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid is through the reaction of boric acid and the corresponding aromatic ether compound under basic conditions. Specific reaction conditions can be adjusted according to actual needs and reaction system.
With regard to safety information, as an organic compound, the use of (3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid should follow the general safety procedures for chemicals. It may be irritating to the skin and eyes, so it is necessary to wear suitable protective equipment during operation. In addition, the compound should be properly stored to prevent accidental reaction with other chemicals or fire. Detailed safety information can be found in the relevant chemical safety data sheets.
(3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid has a wide range of applications in chemical research and organic synthesis. It can be used in the synthesis of boron-containing organic compounds, such as anionic borate esters. These compounds have important applications in drug discovery and ligand design, for example, they act as inhibitors of Tyr-Kinase enzyme activity. In addition,(3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid can also be used as an organic material for optoelectronic devices.
One method for preparing (3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid is through the reaction of boric acid and the corresponding aromatic ether compound under basic conditions. Specific reaction conditions can be adjusted according to actual needs and reaction system.
With regard to safety information, as an organic compound, the use of (3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid should follow the general safety procedures for chemicals. It may be irritating to the skin and eyes, so it is necessary to wear suitable protective equipment during operation. In addition, the compound should be properly stored to prevent accidental reaction with other chemicals or fire. Detailed safety information can be found in the relevant chemical safety data sheets.
Last Update：2024-04-09 20:52:54
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(3-Propoxy-5-(trifluoromethoxy)phenyl)boronic acid
3-氧代-5-氟-3,4-二氢-2H-苯并[B][1,4]噁嗪-6-硼酸频哪醇酯
2-[(2-cyanoethyl)[4-[(2-cyano-4-nitrophenyl)azo]phenyl]amino]ethyl phenoxyacetate
2-全氟辛基溴乙烷
(乙酰氧甲基)三乙氧基硅烷
(5,5-二甲基四氢呋喃-3-基)甲胺盐酸盐
Thiopyrano[2,3-c]pyrrole, 4-methoxy-5,7-dimethyl-, perchlorate (1:1)
TIMTEC-BB SBB010555
Urea, N-[(1R)-3-[5-[(4-fluorophenyl)methyl]-2-thienyl]-1-methyl-2-propyn-1-yl]-N-hydroxy-
Tricyclo[3.3.1.13,7]decane-1-acetamide, N-[2-methyl-5-(9-oxa-3,7-diazabicyclo[3.3.1]non-3-ylcarbonyl)phenyl]-
3-氧代-5-氟-3,4-二氢-2H-苯并[B][1,4]噁嗪-6-硼酸频哪醇酯
2-[(2-cyanoethyl)[4-[(2-cyano-4-nitrophenyl)azo]phenyl]amino]ethyl phenoxyacetate
2-全氟辛基溴乙烷
(乙酰氧甲基)三乙氧基硅烷
(5,5-二甲基四氢呋喃-3-基)甲胺盐酸盐
Thiopyrano[2,3-c]pyrrole, 4-methoxy-5,7-dimethyl-, perchlorate (1:1)
TIMTEC-BB SBB010555
Urea, N-[(1R)-3-[5-[(4-fluorophenyl)methyl]-2-thienyl]-1-methyl-2-propyn-1-yl]-N-hydroxy-
Tricyclo[3.3.1.13,7]decane-1-acetamide, N-[2-methyl-5-(9-oxa-3,7-diazabicyclo[3.3.1]non-3-ylcarbonyl)phenyl]-