(3-fluoro-5-((4-oxopiperidin-1-yl)Methyl)phenyl)boronic acid is a chemical compound that features a boronic acid functional group attached to a phenyl ring. (3-fluoro-5-((4-oxopiperidin-1-yl)Methyl)phenyl)boronic acid is characterized by the presence of a fluorine atom at the 3rd position and a piperidine derivative at the 5th position on the phenyl ring. The boronic acid group endows it with significant value in organic synthesis, especially in Suzuki coupling reactions, which are pivotal for forming carbon-carbon bonds. Moreover, the incorporation of a fluorine atom and a piperidine moiety suggests its potential utility in medicinal chemistry, given the widespread use of fluorine in pharmaceuticals and the recognized biological activity of piperidine-containing compounds. As such, (3-fluoro-5-((4-oxopiperidin-1-yl)Methyl)phenyl)boronic acid holds promise for applications in both organic synthesis and drug development.
1704063-68-2
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Basic information
- Product Name: (3-fluoro-5-((4-oxopiperidin-1-yl)Methyl)phenyl)boronic acid
- Synonyms: (3-fluoro-5-((4-oxopiperidin-1-yl)Methyl)phenyl)boronic acid
- CAS NO:1704063-68-2
- Molecular Formula: C12H15BFNO3
- Molecular Weight: 251.0618032
- EINECS: N/A
- Product Categories: Boronate Ester;Boronic Acid;Potassium Trifluoroborate
- Mol File: 1704063-68-2.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (3-fluoro-5-((4-oxopiperidin-1-yl)Methyl)phenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (3-fluoro-5-((4-oxopiperidin-1-yl)Methyl)phenyl)boronic acid(1704063-68-2)
- EPA Substance Registry System: (3-fluoro-5-((4-oxopiperidin-1-yl)Methyl)phenyl)boronic acid(1704063-68-2)
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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: 1704063-68-2(Hazardous Substances Data)
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1704063-68-2 Usage
Uses
Used in Organic Synthesis:(3-fluoro-5-((4-oxopiperidin-1-yl)Methyl)phenyl)boronic acid is used as a synthetic intermediate for the creation of complex organic molecules. Its boronic acid functional group plays a crucial role in Suzuki coupling reactions, which are widely employed for the formation of carbon-carbon bonds, facilitating the synthesis of a broad range of organic compounds.
Used in Medicinal Chemistry:
In the pharmaceutical industry, (3-fluoro-5-((4-oxopiperidin-1-yl)Methyl)phenyl)boronic acid is used as a building block for the development of new drugs. The presence of a fluorine atom can impart specific properties to the molecule, such as increased lipophilicity and metabolic stability, which are desirable in drug design. Additionally, the piperidine derivative may contribute to the compound's biological activity, making it a candidate for further exploration and optimization in the context of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1704063-68-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,4,0,6 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.Calculate Digit Verification of CAS Registry Number 1704063-68:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*6)+(3*3)+(2*6)+(1*8)=142
142 % 10 = 2
So 1704063-68-2 is a valid CAS Registry Number.
1704063-68-2Upstream product
1704063-68-2Downstream Products
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(3-fluoro-5-((4-oxopiperidin-1-yl)Methyl)phenyl)boronic acid
