(4-(1-(4-((tert-butyldiMethylsilyl)oxy)piperidin-1-yl)ethyl)phenyl)boronic acid is a boronic acid derivative featuring a phenyl and piperidine ring structure, along with a tert-butyldimethylsilyl group. (4-(1-(4-((tert-butyldiMethylsilyl)oxy)piperidin-1-yl)ethyl)phenyl)boronic acid is a valuable building block in organic synthesis due to its ability to participate in Suzuki coupling reactions and other transformations. The presence of the piperidine ring may also contribute to its potential biological activity, as piperidine derivatives are known for their wide range of pharmacological properties.
1704069-37-3
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Basic information
- Product Name: (4-(1-(4-((tert-butyldiMethylsilyl)oxy)piperidin-1-yl)ethyl)phenyl)boronic acid
- Synonyms: (4-(1-(4-((tert-butyldiMethylsilyl)oxy)piperidin-1-yl)ethyl)phenyl)boronic acid
- CAS NO:1704069-37-3
- Molecular Formula: C19H34BNO3Si
- Molecular Weight: 363.37466
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1704069-37-3.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 436.5±55.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.03±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 8.67±0.17(Predicted)
- CAS DataBase Reference: (4-(1-(4-((tert-butyldiMethylsilyl)oxy)piperidin-1-yl)ethyl)phenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (4-(1-(4-((tert-butyldiMethylsilyl)oxy)piperidin-1-yl)ethyl)phenyl)boronic acid(1704069-37-3)
- EPA Substance Registry System: (4-(1-(4-((tert-butyldiMethylsilyl)oxy)piperidin-1-yl)ethyl)phenyl)boronic acid(1704069-37-3)
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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: 1704069-37-3(Hazardous Substances Data)
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1704069-37-3 Usage
Uses
Used in Organic Synthesis:(4-(1-(4-((tert-butyldiMethylsilyl)oxy)piperidin-1-yl)ethyl)phenyl)boronic acid is used as a building block for the synthesis of complex organic molecules. Its boronic acid functionality allows it to participate in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds and the creation of diverse molecular structures.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (4-(1-(4-((tert-butyldiMethylsilyl)oxy)piperidin-1-yl)ethyl)phenyl)boronic acid is used as a starting material for the development of new drugs. The piperidine ring, a common structural element in many bioactive compounds, may impart pharmacological properties to the molecule, making it a promising candidate for the design of novel therapeutic agents.
Used in Chemical Research:
(4-(1-(4-((tert-butyldiMethylsilyl)oxy)piperidin-1-yl)ethyl)phenyl)boronic acid is utilized in chemical research to study the reactivity and properties of boronic acid derivatives. Its unique structure allows researchers to explore various chemical transformations and investigate the potential applications of this class of compounds in different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1704069-37-3 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 9 respectively; the second part has 2 digits, 3 and 7 respectively.Calculate Digit Verification of CAS Registry Number 1704069-37:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*6)+(3*9)+(2*3)+(1*7)=153
153 % 10 = 3
So 1704069-37-3 is a valid CAS Registry Number.
1704069-37-3Upstream product
1704069-37-3Downstream Products
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(4-(1-(4-((tert-butyldiMethylsilyl)oxy)piperidin-1-yl)ethyl)phenyl)boronic acid
