Lithium diisopropylamide solution
2.0 M in THF/n-heptane ethylbenzene, MkSeal
- Product Code: 88702
Alias:
Lithium diisopropylamide; lithium diisopropylamide, lithium diisopropylamide, lithium diisopropylamide, lithium diisopropylamide
CAS:
4111-54-0
| Molecular Weight: | 107.12 g./mol | Molecular Formula: | C₆H₁₄LiN |
|---|---|---|---|
| EC Number: | 223-893-0 | MDL Number: | MFCD00064449 |
| Melting Point: | Boiling Point: | 65℃ | |
| Density: | Storage Condition: | 2~8 ℃ |
Product Description:
Used extensively as a strong, non-nucleophilic base in organic synthesis, it facilitates deprotonation reactions to generate carbanions. Commonly employed in the formation of enolates from carbonyl compounds, which are key intermediates in aldol and Claisen condensations. It is also utilized in the synthesis of pharmaceuticals, agrochemicals, and complex organic molecules. Its ability to selectively deprotonate acidic protons makes it valuable in the preparation of organometallic reagents and in asymmetric synthesis. Often chosen for its solubility in organic solvents and stability at low temperatures, ensuring controlled and efficient reactions.
Product Specification:
| Test | Specification |
|---|---|
| CONCENTRATION TITRATION SEC-BUTANOL | 1.8-2.2 |
| APPEARANCE | YELLOW TO DARK BROWN LIQUID |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 100.000 | 10-20 days | €45.38 |
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| 500.000 | 10-20 days | €119.25 |
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| 1000.000 | 10-20 days | €227.41 |
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Lithium diisopropylamide solution
Used extensively as a strong, non-nucleophilic base in organic synthesis, it facilitates deprotonation reactions to generate carbanions. Commonly employed in the formation of enolates from carbonyl compounds, which are key intermediates in aldol and Claisen condensations. It is also utilized in the synthesis of pharmaceuticals, agrochemicals, and complex organic molecules. Its ability to selectively deprotonate acidic protons makes it valuable in the preparation of organometallic reagents and in asymmetric synthesis. Often chosen for its solubility in organic solvents and stability at low temperatures, ensuring controlled and efficient reactions.
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