2-Isopropoxypyridine-5-boronic acid pinacol ester
97%
- Product Code: 90951
Alias:
6-Isopropoxypyridine-3-boronic acid pinacol ester
CAS:
871839-91-7
Molecular Weight: | 263.15 g./mol | Molecular Formula: | C₁₄H₂₂BNO₃ |
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EC Number: | MDL Number: | MFCD07368871 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It plays a significant role in Suzuki-Miyaura cross-coupling reactions, which are widely employed in organic chemistry to form carbon-carbon bonds. This chemical is valuable in the production of complex molecules, including potential drug candidates for treating various diseases. Additionally, it is utilized in material science for creating advanced organic materials with specific electronic or structural properties. Its boronic ester group makes it a versatile building block in medicinal chemistry and drug discovery research.
Product Specification:
Test | Specification |
---|---|
CARBON BY ELEMENTAL ANALYSIS | 61.5 63.9% |
Melting point | 72 72? |
PURITYHPLC | 97 97% |
APPEARANCE | White to off-white powder or solid or chunks |
INFRARED SPECTROMETRY | Conforms to Structure |
PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿1,746.00 |
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1.000 | 10-20 days | ฿3,951.00 |
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5.000 | 10-20 days | ฿9,657.00 |
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2-Isopropoxypyridine-5-boronic acid pinacol ester
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It plays a significant role in Suzuki-Miyaura cross-coupling reactions, which are widely employed in organic chemistry to form carbon-carbon bonds. This chemical is valuable in the production of complex molecules, including potential drug candidates for treating various diseases. Additionally, it is utilized in material science for creating advanced organic materials with specific electronic or structural properties. Its boronic ester group makes it a versatile building block in medicinal chemistry and drug discovery research.
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