Lithium 4-methyl-1-(pyridin-2-yl)-2,6,7-trioxa-1-borabicyclo[2.2.2]octan-1-uide
95%
- Product Code: 124053
CAS:
1014717-10-2
Molecular Weight: | 230.98 g./mol | Molecular Formula: | C₁₀H₁₅BLiNO₄ |
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EC Number: | MDL Number: | MFCD16038156 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a strong, non-nucleophilic base. Its sterically hindered structure allows it to deprotonate weakly acidic substrates without participating in unwanted side reactions, making it particularly useful in the preparation of sensitive intermediates. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and complex organic molecules where precise control over reactivity is essential. Additionally, its stability and effectiveness in non-polar solvents make it a valuable reagent in anhydrous reaction conditions, facilitating the formation of carbanions and enabling the generation of highly reactive species for further transformations.
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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Lithium 4-methyl-1-(pyridin-2-yl)-2,6,7-trioxa-1-borabicyclo[2.2.2]octan-1-uide
This compound is primarily utilized in organic synthesis as a strong, non-nucleophilic base. Its sterically hindered structure allows it to deprotonate weakly acidic substrates without participating in unwanted side reactions, making it particularly useful in the preparation of sensitive intermediates. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and complex organic molecules where precise control over reactivity is essential. Additionally, its stability and effectiveness in non-polar solvents make it a valuable reagent in anhydrous reaction conditions, facilitating the formation of carbanions and enabling the generation of highly reactive species for further transformations.
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