(3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid is a boronic acid derivative featuring a fluorophenyl group and an ethylpiperazinyl group. This chemical compound is recognized for its potential applications in the pharmaceutical industry, particularly in the synthesis of drug candidates for treating a variety of diseases. Its unique structure and the biological activities associated with boronic acids, such as anti-inflammatory, antiviral, and anticancer properties, make it a valuable asset in medicinal chemistry for designing and creating novel drugs.
1704074-45-2
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Basic information
- Product Name: (3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid
- Synonyms: (3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid
- CAS NO:1704074-45-2
- Molecular Formula: C12H18BFN2O2
- Molecular Weight: 252.0929232
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1704074-45-2.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 438.0±55.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.23±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 7.60±0.10(Predicted)
- CAS DataBase Reference: (3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid(1704074-45-2)
- EPA Substance Registry System: (3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid(1704074-45-2)
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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: 1704074-45-2(Hazardous Substances Data)
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1704074-45-2 Usage
Uses
Used in Pharmaceutical Synthesis:(3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid is used as a building block for the synthesis of pharmaceutical compounds, specifically in the development of potential drug candidates for the treatment of various diseases. Its unique structure allows for the creation of new drugs with improved efficacy and reduced side effects.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid is used as a valuable tool for the design and synthesis of new drugs. Its specific structure and the biological activities of boronic acids contribute to the development of innovative pharmaceuticals with potential applications in treating various medical conditions.
Used in the Development of Fluorescent Sensors:
(3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid is also utilized in the development of fluorescent sensors for various biomolecules. This application highlights the significance of boronic acids in both chemical and biological research, as these sensors can be used to study and detect specific biological targets, contributing to a better understanding of biological processes and the development of targeted therapies.
Used in Antiviral Applications:
(3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid is used as an antiviral agent due to the antiviral properties associated with boronic acids. It can potentially be employed in the development of new antiviral drugs to combat viral infections and diseases.
Used in Anticancer Applications:
In the field of oncology, (3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid is used as a potential anticancer agent. Its structure and biological activities may contribute to the development of new cancer treatments, offering hope for patients suffering from various types of cancer.
Used in Anti-inflammatory Applications:
(3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid is used as an anti-inflammatory agent, leveraging the anti-inflammatory properties of boronic acids. This application can lead to the development of new drugs for the treatment of inflammatory diseases and conditions.
Used in Chemical Research:
In the broader field of chemical research, (3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid is used as a versatile compound for studying various chemical reactions and mechanisms. Its unique structure and properties make it an interesting subject for further exploration and understanding in the realm of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1704074-45-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,4,0,7 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.Calculate Digit Verification of CAS Registry Number 1704074-45:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*7)+(3*4)+(2*4)+(1*5)=142
142 % 10 = 2
So 1704074-45-2 is a valid CAS Registry Number.
1704074-45-2Upstream product
1704074-45-2Downstream Products
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(3-(4-ethylpiperazin-1-yl)-5-fluorophenyl)boronic acid
