2-(4-Methoxythiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 115765
CAS:
1073339-22-6
Molecular Weight: | 240.13 g./mol | Molecular Formula: | C₁₁H₁₇BO₃S |
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EC Number: | MDL Number: | MFCD12405477 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20°C, dark, inert gas |
Product Description:
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its methoxy-thiophene moiety makes it valuable in constructing complex molecules, especially in the synthesis of heterocyclic compounds. Additionally, it is employed in the preparation of organic electronic materials, including polymers and small molecules for optoelectronic applications like OLEDs and organic photovoltaics. Its stability and reactivity make it a versatile tool in medicinal chemistry for drug discovery and development.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,971.00 |
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0.250 | 10-20 days | ฿3,339.00 |
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1.000 | 10-20 days | ฿9,000.00 |
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2-(4-Methoxythiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its methoxy-thiophene moiety makes it valuable in constructing complex molecules, especially in the synthesis of heterocyclic compounds. Additionally, it is employed in the preparation of organic electronic materials, including polymers and small molecules for optoelectronic applications like OLEDs and organic photovoltaics. Its stability and reactivity make it a versatile tool in medicinal chemistry for drug discovery and development.
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