(3-((4-hydroxypiperidin-1-yl)sulfonyl)-4-Methoxyphenyl)boronic acid is a boronic acid derivative with the molecular formula C11H19BNO6S. It features a sulfurand nitrogen-containing functional group, a methoxyphenyl group, and a piperidine ring. This chemical compound is known for its utility in organic synthesis and pharmaceutical research.
1704081-13-9
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Basic information
- Product Name: (3-((4-hydroxypiperidin-1-yl)sulfonyl)-4-Methoxyphenyl)boronic acid
- Synonyms: (3-((4-hydroxypiperidin-1-yl)sulfonyl)-4-Methoxyphenyl)boronic acid
- CAS NO:1704081-13-9
- Molecular Formula: C12H18BNO6S
- Molecular Weight: 315.15042
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1704081-13-9.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-((4-hydroxypiperidin-1-yl)sulfonyl)-4-Methoxyphenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (3-((4-hydroxypiperidin-1-yl)sulfonyl)-4-Methoxyphenyl)boronic acid(1704081-13-9)
- EPA Substance Registry System: (3-((4-hydroxypiperidin-1-yl)sulfonyl)-4-Methoxyphenyl)boronic acid(1704081-13-9)
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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: 1704081-13-9(Hazardous Substances Data)
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1704081-13-9 Usage
Uses
Used in Organic Synthesis:(3-((4-hydroxypiperidin-1-yl)sulfonyl)-4-Methoxyphenyl)boronic acid is used as a building block in organic synthesis for the creation of various biologically active molecules. Its unique structure allows for the formation of complex organic molecules through chemical reactions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3-((4-hydroxypiperidin-1-yl)sulfonyl)-4-Methoxyphenyl)boronic acid is used as a key component in the synthesis of pharmaceutical compounds. Its potential applications in medicinal chemistry and drug discovery research make it a valuable asset for developing new drugs and therapies.
Used in Suzuki-Miyaura Coupling Reactions:
(3-((4-hydroxypiperidin-1-yl)sulfonyl)-4-Methoxyphenyl)boronic acid is utilized as a coupling agent in Suzuki-Miyaura coupling reactions, which are widely employed in the synthesis of complex organic molecules. This reaction is particularly important in the fields of organic chemistry and materials science, as it allows for the formation of carbon-carbon bonds, a crucial aspect in the construction of molecular structures.
Check Digit Verification of cas no
The CAS Registry Mumber 1704081-13-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,4,0,8 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.Calculate Digit Verification of CAS Registry Number 1704081-13:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*8)+(3*1)+(2*1)+(1*3)=129
129 % 10 = 9
So 1704081-13-9 is a valid CAS Registry Number.
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(3-((4-hydroxypiperidin-1-yl)sulfonyl)-4-Methoxyphenyl)boronic acid
