2-3-[(4-bromo-2-chlorophenoxy)methyl]phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 83714
CAS:
2246646-61-5
Molecular Weight: | 423.53624 g./mol | Molecular Formula: | C₁₉H₂₁BBrClO₃ |
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EC Number: | MDL Number: | MFCD32206528 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis as a key intermediate for the preparation of complex molecules. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to construct carbon-carbon bonds for drug development. Additionally, it serves as a building block in the synthesis of agrochemicals, enabling the creation of compounds with potential herbicidal or pesticidal properties. Its aromatic structure also lends itself to applications in materials science, particularly in the development of organic electronic materials or polymers. Researchers may also use it in the study of boron-containing compounds for their unique reactivity and potential therapeutic applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.025 | 10-20 days | ฿2,736.00 |
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0.100 | 10-20 days | ฿8,190.00 |
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2-3-[(4-bromo-2-chlorophenoxy)methyl]phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily utilized in organic synthesis as a key intermediate for the preparation of complex molecules. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to construct carbon-carbon bonds for drug development. Additionally, it serves as a building block in the synthesis of agrochemicals, enabling the creation of compounds with potential herbicidal or pesticidal properties. Its aromatic structure also lends itself to applications in materials science, particularly in the development of organic electronic materials or polymers. Researchers may also use it in the study of boron-containing compounds for their unique reactivity and potential therapeutic applications.
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