(2-(Thiomorpholinomethyl)phenyl)boronic acid
95%
- Product Code: 80015
CAS:
1158941-47-9
Molecular Weight: | 237.13 g./mol | Molecular Formula: | C₁₁H₁₆BNO₂S |
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EC Number: | MDL Number: | MFCD12025994 | |
Melting Point: | Boiling Point: | 426.2±55.0 °C at 760 mmHg | |
Density: | Storage Condition: | 2-8℃, dry, airtight |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is pivotal in Suzuki-Miyaura cross-coupling reactions. These reactions are instrumental in forming carbon-carbon bonds, a fundamental step in the synthesis of complex organic molecules, including potential drug candidates. Additionally, the thiomorpholine moiety can enhance the compound's binding affinity to biological targets, making it valuable in the development of enzyme inhibitors or receptor modulators. Its unique structure also allows for potential applications in the design of boron-based therapeutics, which are explored for their anti-inflammatory, anti-cancer, and anti-infective properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | €118.24 |
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0.250 | 10-20 days | €393.67 |
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1.000 | 10-20 days | €1,068.23 |
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(2-(Thiomorpholinomethyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is pivotal in Suzuki-Miyaura cross-coupling reactions. These reactions are instrumental in forming carbon-carbon bonds, a fundamental step in the synthesis of complex organic molecules, including potential drug candidates. Additionally, the thiomorpholine moiety can enhance the compound's binding affinity to biological targets, making it valuable in the development of enzyme inhibitors or receptor modulators. Its unique structure also allows for potential applications in the design of boron-based therapeutics, which are explored for their anti-inflammatory, anti-cancer, and anti-infective properties.
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