(4-((Dipropylamino)methyl)phenyl)boronic acid
95%
- Product Code: 46450
CAS:
1333121-80-4
Molecular Weight: | 235.13028 g./mol | Molecular Formula: | C₁₃H₂₂BNO₂ |
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Density: | Storage Condition: | room temperature |
Product Description:
(4-((Dipropylamino)methyl)phenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical and materials science industries to form carbon-carbon bonds, enabling the synthesis of complex organic molecules. The compound serves as a boronic acid reagent, facilitating the coupling of aryl or vinyl halides with aryl or vinyl boronic acids to produce biaryl or styrene derivatives. Its application is crucial in the development of drugs, agrochemicals, and advanced materials, where precise molecular construction is required. Additionally, the dipropylamino group in its structure can enhance solubility and reactivity in certain reaction conditions, making it a versatile tool in synthetic chemistry.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | £157.14 |
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0.250 | 10-20 days | £262.18 |
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1.000 | 10-20 days | £526.80 |
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(4-((Dipropylamino)methyl)phenyl)boronic acid
(4-((Dipropylamino)methyl)phenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical and materials science industries to form carbon-carbon bonds, enabling the synthesis of complex organic molecules. The compound serves as a boronic acid reagent, facilitating the coupling of aryl or vinyl halides with aryl or vinyl boronic acids to produce biaryl or styrene derivatives. Its application is crucial in the development of drugs, agrochemicals, and advanced materials, where precise molecular construction is required. Additionally, the dipropylamino group in its structure can enhance solubility and reactivity in certain reaction conditions, making it a versatile tool in synthetic chemistry.
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