(2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid is a boronic acid derivative with the molecular formula C14H12BF3O4. It features a benzene ring with an attached benzyloxy group and a trifluoromethoxy group, making it a versatile compound in organic chemistry.
Used in Pharmaceutical Industry:
(2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid is used as a building block or reagent for the synthesis of various pharmaceuticals. Its ability to form stable complexes with diols and participate in Suzuki-Miyaura cross-coupling reactions facilitates the formation of carbon-carbon bonds, which is crucial in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, (2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid serves as a key component in the synthesis of agrochemicals. Its reactivity and stability make it suitable for creating compounds that can be used in pest control and crop protection.
Used in Materials Science:
(2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid is used as a reagent in the development of new materials. Its unique properties allow it to be incorporated into the synthesis of advanced materials with specific characteristics, such as improved strength, flexibility, or chemical resistance.
Used in Cancer Therapy Research:
(2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid is studied for its potential applications in cancer therapy. It has shown the ability to inhibit certain enzymes and biological pathways, making it a promising candidate for the development of new treatments for various types of cancer.
Used in Other Medical Treatments:
Beyond cancer therapy, (2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid is also being investigated for its potential use in other medical treatments. Its ability to interact with biological systems and inhibit specific pathways suggests it may have applications in treating a range of diseases and conditions.
Used in Pharmaceutical Industry:
(2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid is used as a building block or reagent for the synthesis of various pharmaceuticals. Its ability to form stable complexes with diols and participate in Suzuki-Miyaura cross-coupling reactions facilitates the formation of carbon-carbon bonds, which is crucial in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, (2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid serves as a key component in the synthesis of agrochemicals. Its reactivity and stability make it suitable for creating compounds that can be used in pest control and crop protection.
Used in Materials Science:
(2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid is used as a reagent in the development of new materials. Its unique properties allow it to be incorporated into the synthesis of advanced materials with specific characteristics, such as improved strength, flexibility, or chemical resistance.
Used in Cancer Therapy Research:
(2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid is studied for its potential applications in cancer therapy. It has shown the ability to inhibit certain enzymes and biological pathways, making it a promising candidate for the development of new treatments for various types of cancer.
Used in Other Medical Treatments:
Beyond cancer therapy, (2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid is also being investigated for its potential use in other medical treatments. Its ability to interact with biological systems and inhibit specific pathways suggests it may have applications in treating a range of diseases and conditions.
1704064-19-6
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Basic information
- Product Name: (2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid
- Synonyms: (2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid
- CAS NO:1704064-19-6
- Molecular Formula: C14H12BF3O4
- Molecular Weight: 312.0488896
- EINECS: N/A
- Product Categories: Boronate Ester;Boronic Acid;Potassium Trifluoroborate
- Mol File: 1704064-19-6.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 424.7±55.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.37±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 8.34±0.53(Predicted)
- CAS DataBase Reference: (2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid(1704064-19-6)
- EPA Substance Registry System: (2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid(1704064-19-6)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 1704064-19-6(Hazardous Substances Data)
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1704064-19-6 Usage
Check Digit Verification of cas no
The CAS Registry Mumber 1704064-19-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,4,0,6 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.Calculate Digit Verification of CAS Registry Number 1704064-19:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*6)+(3*4)+(2*1)+(1*9)=136
136 % 10 = 6
So 1704064-19-6 is a valid CAS Registry Number.
1704064-19-6Upstream product
1704064-19-6Downstream Products
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(2-(benzyloxy)-4-(trifluoroMethoxy)phenyl)boronic acid
