(4-bromo-3-p-tolyl-isoxazol-5-yl)-boronic acid is a chemical compound that features a boronic acid functional group and an isoxazole ring. (4-bromo-3-p-tolyl-isoxazol-5-yl)-boronic acid is known for its ability to form stable complexes with diols and other Lewis bases, which makes it a versatile building block in the field of organic chemistry and pharmaceutical production.
14399-52-1
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Basic information
- Product Name: (4-bromo-3-p-tolyl-isoxazol-5-yl)-boronic acid
- Synonyms:
- CAS NO:14399-52-1
- Molecular Formula:
- Molecular Weight: 281.901
- EINECS: N/A
- Product Categories: N/A
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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-p-tolyl-isoxazol-5-yl)-boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (4-bromo-3-p-tolyl-isoxazol-5-yl)-boronic acid(14399-52-1)
- EPA Substance Registry System: (4-bromo-3-p-tolyl-isoxazol-5-yl)-boronic acid(14399-52-1)
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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: 14399-52-1(Hazardous Substances Data)
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14399-52-1 Usage
Uses
Used in Organic Synthesis:(4-bromo-3-p-tolyl-isoxazol-5-yl)-boronic acid is used as a reagent in organic synthesis for its ability to form stable complexes with diols and other Lewis bases. This property allows it to be a key component in creating a variety of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (4-bromo-3-p-tolyl-isoxazol-5-yl)-boronic acid serves as a valuable building block. Its unique structure and functional groups enable the development of new drugs with potential therapeutic applications.
Used in Cross-Coupling Reactions:
The boronic acid functionality of (4-bromo-3-p-tolyl-isoxazol-5-yl)-boronic acid makes it particularly useful in Suzuki-Miyaura coupling reactions, which are widely employed in the synthesis of biologically active compounds and natural products.
Used in Chemical Transformations:
The presence of the isoxazole ring in (4-bromo-3-p-tolyl-isoxazol-5-yl)-boronic acid provides additional versatility, as it can participate in various chemical transformations, further expanding the compound's utility in creating diverse chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 14399-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,9 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.Calculate Digit Verification of CAS Registry Number 14399-52:
(7*1)+(6*4)+(5*3)+(4*9)+(3*9)+(2*5)+(1*2)=121
121 % 10 = 1
So 14399-52-1 is a valid CAS Registry Number.
14399-52-1Upstream product
14399-52-1Downstream Products
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(4-bromo-3-p-tolyl-isoxazol-5-yl)-boronic acid
