(3-(N-MethoxysulfaMoyl)phenyl)boronic acid is a chemical compound characterized by the presence of a boronic acid functional group and a methoxysulfamoyl group attached to a phenyl ring. (3-(N-MethoxysulfaMoyl)phenyl)boronic acid is known for its role in organic synthesis and its potential applications in medicinal chemistry, particularly as an anticancer agent.
1704066-72-7
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Basic information
- Product Name: (3-(N-MethoxysulfaMoyl)phenyl)boronic acid
- Synonyms: (3-(N-MethoxysulfaMoyl)phenyl)boronic acid
- CAS NO:1704066-72-7
- Molecular Formula: C7H10BNO5S
- Molecular Weight: 231.034
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1704066-72-7.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 442.2±55.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.46±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 6.27±0.40(Predicted)
- CAS DataBase Reference: (3-(N-MethoxysulfaMoyl)phenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (3-(N-MethoxysulfaMoyl)phenyl)boronic acid(1704066-72-7)
- EPA Substance Registry System: (3-(N-MethoxysulfaMoyl)phenyl)boronic acid(1704066-72-7)
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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: 1704066-72-7(Hazardous Substances Data)
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1704066-72-7 Usage
Uses
Used in Organic Synthesis:(3-(N-MethoxysulfaMoyl)phenyl)boronic acid is used as a reagent for the formation of carbon-carbon and carbon-nitrogen bonds in organic synthesis. Its unique structure allows for versatile reactions and the creation of a wide range of molecular structures.
Used in Medicinal Chemistry:
In the pharmaceutical industry, (3-(N-MethoxysulfaMoyl)phenyl)boronic acid is used as a potential anticancer agent. It has demonstrated the ability to inhibit the activity of certain enzymes that play a role in cancer progression, making it a promising candidate for further research and development in cancer treatment.
Used in Sensor and Diagnostic Tool Development:
Boronic acids, including (3-(N-MethoxysulfaMoyl)phenyl)boronic acid, have been extensively studied for their potential use in the development of sensors and diagnostic tools. Their unique chemical properties make them suitable for detecting and interacting with specific biological targets, which can be beneficial in various research and medical applications.
Overall, (3-(N-MethoxysulfaMoyl)phenyl)boronic acid has a broad range of potential applications across the chemical, pharmaceutical, and biological research industries, making it a valuable compound for further exploration and development.
Check Digit Verification of cas no
The CAS Registry Mumber 1704066-72-7 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 6 respectively; the second part has 2 digits, 7 and 2 respectively.Calculate Digit Verification of CAS Registry Number 1704066-72:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*6)+(3*6)+(2*7)+(1*2)=147
147 % 10 = 7
So 1704066-72-7 is a valid CAS Registry Number.
1704066-72-7Upstream product
1704066-72-7Downstream Products
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(3-(N-MethoxysulfaMoyl)phenyl)boronic acid
