(3-(pyrrolidin-1-ylsulfonyl)-4-(trifluoroMethoxy)phenyl)boronic acid is an organoboron compound that features a boronic acid functional group. It is widely utilized in organic synthesis as a reagent for cross-coupling reactions, which are crucial for creating carbon-carbon and carbon-heteroatom bonds. The presence of pyrrolidin-1-ylsulfonyl and trifluoromethoxy groups enhances the compound's reactivity and stability, making it a valuable asset in medicinal chemistry and drug discovery. Additionally, this chemical has demonstrated potential applications in the fields of materials science and catalysis, showcasing its versatility and diverse uses in organic chemistry.
1704069-27-1
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Basic information
- Product Name: (3-(pyrrolidin-1-ylsulfonyl)-4-(trifluoroMethoxy)phenyl)boronic acid
- Synonyms: (3-(pyrrolidin-1-ylsulfonyl)-4-(trifluoroMethoxy)phenyl)boronic acid
- CAS NO:1704069-27-1
- Molecular Formula: C11H13BF3NO5S
- Molecular Weight: 339.0958296
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1704069-27-1.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 477.9±55.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.55±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 7.19±0.10(Predicted)
- CAS DataBase Reference: (3-(pyrrolidin-1-ylsulfonyl)-4-(trifluoroMethoxy)phenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (3-(pyrrolidin-1-ylsulfonyl)-4-(trifluoroMethoxy)phenyl)boronic acid(1704069-27-1)
- EPA Substance Registry System: (3-(pyrrolidin-1-ylsulfonyl)-4-(trifluoroMethoxy)phenyl)boronic acid(1704069-27-1)
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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: 1704069-27-1(Hazardous Substances Data)
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1704069-27-1 Usage
Uses
Used in Organic Synthesis:(3-(pyrrolidin-1-ylsulfonyl)-4-(trifluoroMethoxy)phenyl)boronic acid is used as a reagent in organic synthesis for facilitating cross-coupling reactions. Its application is essential for forming carbon-carbon and carbon-heteroatom bonds, which are vital in constructing complex molecular structures.
Used in Medicinal Chemistry and Drug Discovery:
In the pharmaceutical industry, (3-(pyrrolidin-1-ylsulfonyl)-4-(trifluoroMethoxy)phenyl)boronic acid is employed as a key component in the development of new drugs. Its high reactivity and stability make it an ideal candidate for creating novel molecular entities with potential therapeutic applications.
Used in Materials Science:
(3-(pyrrolidin-1-ylsulfonyl)-4-(trifluoroMethoxy)phenyl)boronic acid is also utilized in materials science, where it contributes to the development of new materials with enhanced properties. Its unique chemical structure allows for the creation of materials with improved performance in various applications.
Used in Catalysis:
(3-(pyrrolidin-1-ylsulfonyl)-4-(trifluoroMethoxy)phenyl)boronic acid has demonstrated potential applications in catalysis, where it can be used to accelerate chemical reactions. Its presence can enhance the efficiency of various industrial processes, leading to more sustainable and cost-effective production methods.
Check Digit Verification of cas no
The CAS Registry Mumber 1704069-27-1 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, 2 and 7 respectively.Calculate Digit Verification of CAS Registry Number 1704069-27:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*6)+(3*9)+(2*2)+(1*7)=151
151 % 10 = 1
So 1704069-27-1 is a valid CAS Registry Number.
1704069-27-1Upstream product
1704069-27-1Downstream Products
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(3-(pyrrolidin-1-ylsulfonyl)-4-(trifluoroMethoxy)phenyl)boronic acid
