Phenyllithium solution
1.0 M solution in ethyl ether, MkSeal
- Product Code: 88711
Alias:
Phenyllithium
CAS:
591-51-5
| Molecular Weight: | 84.04 g./mol | Molecular Formula: | C₆H₅Li |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00014254 | |
| Melting Point: | Boiling Point: | 140-143 °C | |
| Density: | 0.835 g/mL at 25 °C | Storage Condition: | 2~8°C |
Product Description:
Phenyllithium solution is widely used in organic synthesis as a strong base and nucleophile. It is particularly valuable in the formation of carbon-carbon bonds through reactions such as nucleophilic addition and substitution. In pharmaceutical research, it is employed to synthesize complex organic molecules, including intermediates for drug development. The solution is also utilized in polymer chemistry to initiate polymerization processes, leading to the creation of specialized polymers. Additionally, it plays a role in the preparation of organometallic compounds, which are essential in catalysis and material science. Its reactivity with carbonyl compounds makes it a key reagent in the synthesis of alcohols, ketones, and other derivatives.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | DARK BROWN TO BLACK LIQUID |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 25.000 | 10-20 days | $83.47 |
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Phenyllithium solution
Phenyllithium solution is widely used in organic synthesis as a strong base and nucleophile. It is particularly valuable in the formation of carbon-carbon bonds through reactions such as nucleophilic addition and substitution. In pharmaceutical research, it is employed to synthesize complex organic molecules, including intermediates for drug development. The solution is also utilized in polymer chemistry to initiate polymerization processes, leading to the creation of specialized polymers. Additionally, it plays a role in the preparation of organometallic compounds, which are essential in catalysis and material science. Its reactivity with carbonyl compounds makes it a key reagent in the synthesis of alcohols, ketones, and other derivatives.
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