5868-55-3
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Basic information
- Product Name: (3-p-tolyl-isoxazol-5-yl)-boronic acid
- Synonyms:
- CAS NO:5868-55-3
- Molecular Formula:
- Molecular Weight: 203.005
- EINECS: N/A
- Product Categories: N/A
- Mol File: 5868-55-3.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: (3-p-tolyl-isoxazol-5-yl)-boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (3-p-tolyl-isoxazol-5-yl)-boronic acid(5868-55-3)
- EPA Substance Registry System: (3-p-tolyl-isoxazol-5-yl)-boronic acid(5868-55-3)
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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: 5868-55-3(Hazardous Substances Data)
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5868-55-3 Usage
Description
(3-p-tolyl-isoxazol-5-yl)-boronic acid is a chemical compound characterized by an isoxazole ring fused with a p-tolyl group and a boronic acid group. This unique structure endows it with distinctive reactivity and potential applications in various fields.Used in Pharmaceutical Research:
(3-p-tolyl-isoxazol-5-yl)-boronic acid is utilized as a building block for the development of new pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of complex organic molecules with potential therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, (3-p-tolyl-isoxazol-5-yl)-boronic acid serves as a valuable intermediate. Its boronic acid functional group is particularly advantageous for Suzuki-Miyaura cross-coupling reactions, a widely used method for creating carbon-carbon bonds in the assembly of complex organic molecules.
Used in Materials Science:
(3-p-tolyl-isoxazol-5-yl)-boronic acid also finds applications in materials science. Its incorporation into new materials can lead to the development of advanced materials with unique properties, such as improved strength, stability, or specific interactions with biological systems.
Overall, (3-p-tolyl-isoxazol-5-yl)-boronic acid is a versatile chemical entity with broad applications across different industries, primarily due to its distinctive structure and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 5868-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,6 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.Calculate Digit Verification of CAS Registry Number 5868-55:
(6*5)+(5*8)+(4*6)+(3*8)+(2*5)+(1*5)=133
133 % 10 = 3
So 5868-55-3 is a valid CAS Registry Number.
5868-55-3Upstream product
5868-55-3Downstream Products
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(3-p-tolyl-isoxazol-5-yl)-boronic acid
