(3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)boronic acid is a chemical compound that plays a significant role in organic synthesis and pharmaceutical research. It features a boronic acid group, which is instrumental in Suzuki coupling reactions for the formation of carbon-carbon bonds. The incorporation of a trifluoromethyl group imparts distinctive properties to the molecule, enhancing its utility in the creation of innovative drugs and agrochemicals. The pyrrolidin-1-yl group present in the compound indicates its potential as a building block in the synthesis of biologically active molecules. In essence, (3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)boronic acid is a multifaceted and beneficial chemical entity that significantly contributes to the progress of organic chemistry and drug discovery.
1704067-30-0
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Basic information
- Product Name: (3-(pyrrolidin-1-yl)-5-(trifluoroMethyl)phenyl)boronic acid
- Synonyms: (3-(pyrrolidin-1-yl)-5-(trifluoroMethyl)phenyl)boronic acid
- CAS NO:1704067-30-0
- Molecular Formula: C11H13BF3NO2
- Molecular Weight: 259.0326296
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1704067-30-0.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 411.5±55.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.34±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 7.58±0.10(Predicted)
- CAS DataBase Reference: (3-(pyrrolidin-1-yl)-5-(trifluoroMethyl)phenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (3-(pyrrolidin-1-yl)-5-(trifluoroMethyl)phenyl)boronic acid(1704067-30-0)
- EPA Substance Registry System: (3-(pyrrolidin-1-yl)-5-(trifluoroMethyl)phenyl)boronic acid(1704067-30-0)
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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: 1704067-30-0(Hazardous Substances Data)
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1704067-30-0 Usage
Uses
Used in Organic Synthesis:(3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)boronic acid is utilized as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structural features facilitate the development of new synthetic pathways and methodologies.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)boronic acid is employed as a building block for the synthesis of biologically active compounds. Its presence in drug candidates can potentially lead to the discovery of new therapeutic agents with improved pharmacological properties.
Used in Drug Development:
(3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)boronic acid is used as a structural component in the development of novel drugs and agrochemicals. The trifluoromethyl group adds specific characteristics that can enhance the potency, selectivity, and metabolic stability of the resulting compounds.
Used in Suzuki Coupling Reactions:
As a boronic acid derivative, (3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)boronic acid is used as a coupling partner in Suzuki reactions to form carbon-carbon bonds. This application is crucial for the assembly of complex molecular frameworks and the synthesis of diverse organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1704067-30-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,4,0,6 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.Calculate Digit Verification of CAS Registry Number 1704067-30:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*6)+(3*7)+(2*3)+(1*0)=140
140 % 10 = 0
So 1704067-30-0 is a valid CAS Registry Number.
1704067-30-0Upstream product
1704067-30-0Downstream Products
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(3-(pyrrolidin-1-yl)-5-(trifluoroMethyl)phenyl)boronic acid
