2-(3-(Benzyloxy)-4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
≥95%
- Product Code: 62337
CAS:
1005010-03-6
| Molecular Weight: | 340.22 g./mol | Molecular Formula: | C₂₀H₂₅BO₄ |
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| EC Number: | MDL Number: | MFCD05663840 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as a boron-containing intermediate. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the formation of carbon-carbon bonds, particularly in the synthesis of complex organic molecules such as pharmaceuticals, agrochemicals, and advanced materials. Its structure, featuring a dioxaborolane group, makes it a stable and efficient reagent for introducing aryl or heteroaryl groups into target molecules. Additionally, it is used in the development of bioactive compounds and in the preparation of polymers with specific electronic or optical properties. Its applications extend to the field of medicinal chemistry, where it aids in the creation of drug candidates with potential therapeutic effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $634.01 |
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| 1.000 | 10-20 days | $1,268.03 |
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2-(3-(Benzyloxy)-4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily utilized in organic synthesis as a boron-containing intermediate. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the formation of carbon-carbon bonds, particularly in the synthesis of complex organic molecules such as pharmaceuticals, agrochemicals, and advanced materials. Its structure, featuring a dioxaborolane group, makes it a stable and efficient reagent for introducing aryl or heteroaryl groups into target molecules. Additionally, it is used in the development of bioactive compounds and in the preparation of polymers with specific electronic or optical properties. Its applications extend to the field of medicinal chemistry, where it aids in the creation of drug candidates with potential therapeutic effects.
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