Lithium 2,2,6,6-tetramethylpiperidide
97%
- Product Code: 78409
CAS:
38227-87-1
| Molecular Weight: | 147.19 g./mol | Molecular Formula: | C₉H₁₈LiN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00015910 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry, inert gas |
Product Description:
Used as a strong, non-nucleophilic base in organic synthesis, particularly for deprotonating weakly acidic substrates. It is highly effective in generating carbanions, which are intermediates in various reactions like alkylations, acylations, and condensations. Commonly employed in the preparation of organolithium compounds and in the synthesis of complex molecules, including pharmaceuticals and fine chemicals. Its sterically hindered structure minimizes side reactions, making it a valuable reagent in selective transformations.
Product Specification:
| Test | Specification |
|---|---|
| Titration by Sec-Butanol | 96.5-103.5 |
| Appearance | Faint Yellow to Dark Yellow and Faint Brown to Dark Brown;Powder or Solid or Chunk(s) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,820.00 |
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| 5.000 | 10-20 days | ฿7,300.00 |
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| 10.000 | 10-20 days | ฿14,120.00 |
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Lithium 2,2,6,6-tetramethylpiperidide
Used as a strong, non-nucleophilic base in organic synthesis, particularly for deprotonating weakly acidic substrates. It is highly effective in generating carbanions, which are intermediates in various reactions like alkylations, acylations, and condensations. Commonly employed in the preparation of organolithium compounds and in the synthesis of complex molecules, including pharmaceuticals and fine chemicals. Its sterically hindered structure minimizes side reactions, making it a valuable reagent in selective transformations.
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