N-(6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazol-2-yl)acetamide
97%
- Product Code: 67344
CAS:
885069-14-7
Molecular Weight: | 318.20 g./mol | Molecular Formula: | C₁₅H₁₉BN₂O₃S |
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EC Number: | MDL Number: | MFCD22571502 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura reactions, where it serves as a boronate ester intermediate. Its structure, featuring a benzo[d]thiazole core, makes it valuable in the development of pharmaceuticals and agrochemicals, as it can act as a building block for biologically active molecules. Additionally, the acetamide group enhances its potential in medicinal chemistry, where it can be modified to create compounds with specific therapeutic properties, such as anti-inflammatory or antimicrobial agents. Its boronate ester functionality also allows for its use in material science, particularly in the design of advanced polymers and sensors.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | ฿7,425.00 |
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0.250 | 10-20 days | ฿26,343.00 |
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N-(6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazol-2-yl)acetamide
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura reactions, where it serves as a boronate ester intermediate. Its structure, featuring a benzo[d]thiazole core, makes it valuable in the development of pharmaceuticals and agrochemicals, as it can act as a building block for biologically active molecules. Additionally, the acetamide group enhances its potential in medicinal chemistry, where it can be modified to create compounds with specific therapeutic properties, such as anti-inflammatory or antimicrobial agents. Its boronate ester functionality also allows for its use in material science, particularly in the design of advanced polymers and sensors.
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