(2-Methoxy-5-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid is a boronic acid compound with a molecular formula of C13H18BNO5S. It is characterized by its unique structure, which includes a methoxy group at the 2nd position and a pyrrolidin-1-ylsulfonyl group at the 5th position of the phenyl ring. (2-Methoxy-5-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid is a derivative of boronic acid, which endows it with specific reactivity and properties.
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Basic information
- Product Name: (2-Methoxy-5-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid
- Synonyms: (2-Methoxy-5-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid
- CAS NO:1704080-33-0
- Molecular Formula: C11H16BNO5S
- Molecular Weight: 285.12444
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1704080-33-0.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: (2-Methoxy-5-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (2-Methoxy-5-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid(1704080-33-0)
- EPA Substance Registry System: (2-Methoxy-5-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid(1704080-33-0)
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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: 1704080-33-0(Hazardous Substances Data)
1704080-33-0 Usage
Uses
Used in Organic Synthesis:(2-Methoxy-5-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid is used as a building block in organic synthesis for the creation of complex organic molecules. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of various organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2-Methoxy-5-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid is utilized as a key intermediate in the development of pharmaceuticals. Its reactivity and structural features contribute to the design and synthesis of novel drug candidates with potential therapeutic applications.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
(2-Methoxy-5-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid is used as a reactant in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the formation of carbon-carbon bonds. This reaction is crucial for the synthesis of various organic compounds, including those with pharmaceutical relevance.
Used in Disease Treatment Research:
Due to its unique structure and reactivity, (2-Methoxy-5-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid is a potential candidate for the treatment of various diseases and conditions. Its application in this area is still under research, but it holds promise for future therapeutic developments.
Overall, (2-Methoxy-5-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid is a versatile and valuable chemical compound with applications in organic synthesis, medicinal chemistry, and potentially in the treatment of diseases. Its unique properties and reactivity make it an important tool in the hands of researchers and chemists working towards the development of new pharmaceuticals and organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1704080-33-0 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 0 respectively; the second part has 2 digits, 3 and 3 respectively.Calculate Digit Verification of CAS Registry Number 1704080-33:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*8)+(3*0)+(2*3)+(1*3)=130
130 % 10 = 0
So 1704080-33-0 is a valid CAS Registry Number.
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(2-Methoxy-5-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid
