13271-76-6
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Basic information
- Product Name: (4-bromo-3-phenyl-isoxazol-5-yl)-boronic acid
- Synonyms:
- CAS NO:13271-76-6
- Molecular Formula:
- Molecular Weight: 267.874
- EINECS: N/A
- Product Categories: N/A
- Mol File: 13271-76-6.mol
- Article Data: 0
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (4-bromo-3-phenyl-isoxazol-5-yl)-boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (4-bromo-3-phenyl-isoxazol-5-yl)-boronic acid(13271-76-6)
- EPA Substance Registry System: (4-bromo-3-phenyl-isoxazol-5-yl)-boronic acid(13271-76-6)
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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: 13271-76-6(Hazardous Substances Data)
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13271-76-6 Usage
Description
(4-bromo-3-phenyl-isoxazol-5-yl)-boronic acid is a chemical compound characterized by the presence of a boronic acid functional group attached to an isoxazole ring, which features a bromine and a phenyl group as substituents. (4-bromo-3-phenyl-isoxazol-5-yl)-boronic acid is recognized for its ability to form stable complexes with diols and amines, a property that makes it a versatile tool in the formation of carbon-carbon and carbon-heteroatom bonds in chemical reactions.Uses
Used in Organic Synthesis:(4-bromo-3-phenyl-isoxazol-5-yl)-boronic acid is used as a reagent in organic synthesis for its capacity to facilitate the formation of carbon-carbon and carbon-heteroatom bonds, which are crucial in constructing complex molecular structures.
Used in Pharmaceutical Compound Design:
In the pharmaceutical industry, (4-bromo-3-phenyl-isoxazol-5-yl)-boronic acid serves as a building block for designing and preparing pharmaceutical compounds. Its unique structure and functional groups make it a promising candidate for the development of new drugs to treat various diseases.
Used in Medicinal Chemistry:
(4-bromo-3-phenyl-isoxazol-5-yl)-boronic acid is utilized in medicinal chemistry for its potential applications in the creation of novel therapeutic agents. Its ability to form stable complexes with other molecules can be harnessed to develop drugs with improved efficacy and selectivity.
Used in Material Science:
(4-bromo-3-phenyl-isoxazol-5-yl)-boronic acid has been studied for its potential use in material science, where its unique properties could contribute to the development of new materials with specific characteristics, such as enhanced stability or reactivity.
Used as a Ligand in Catalysis:
(4-bromo-3-phenyl-isoxazol-5-yl)-boronic acid also has potential applications as a ligand in catalysis, where it could be employed to improve the efficiency and selectivity of catalytic reactions, leading to more sustainable and cost-effective chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 13271-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,7 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.Calculate Digit Verification of CAS Registry Number 13271-76:
(7*1)+(6*3)+(5*2)+(4*7)+(3*1)+(2*7)+(1*6)=86
86 % 10 = 6
So 13271-76-6 is a valid CAS Registry Number.
13271-76-6Upstream product
13271-76-6Downstream Products
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(4-bromo-3-phenyl-isoxazol-5-yl)-boronic acid
