2-Methoxypropene
98%
- Product Code: 205391
Alias:
Methisopropenyl ether
CAS:
116-11-0
| Molecular Weight: | 72.11 g./mol | Molecular Formula: | CH₂=C(CH₃)OCH₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00014929 | |
| Melting Point: | Boiling Point: | 34-36 °C | |
| Density: | 0.753 g/mL | Storage Condition: | 2~8°C |
Product Description:
Used primarily as a protecting group reagent in organic synthesis, particularly for masking carbonyl groups during multistep syntheses. It reacts readily with aldehydes and ketones under mild acidic conditions to form methoxy enol ethers, which are stable under basic conditions and resist nucleophilic attack. This allows selective transformation of other functional groups in the molecule without affecting the carbonyl. After the desired reactions are complete, the protecting group can be removed easily using aqueous acid, regenerating the original carbonyl compound. Its volatility and reactivity make it suitable for use in anhydrous environments where controlled, reversible protection is needed. Also employed in the synthesis of fragrances and pharmaceuticals where precise functional group manipulation is critical.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5ml | 10-20 days | ฿300.00 |
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| 25ml | 10-20 days | ฿520.00 |
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| 100ml | 10-20 days | ฿730.00 |
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| 500ml | 10-20 days | ฿2,360.00 |
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| 2.5L | 10-20 days | ฿8,200.00 |
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2-Methoxypropene
Used primarily as a protecting group reagent in organic synthesis, particularly for masking carbonyl groups during multistep syntheses. It reacts readily with aldehydes and ketones under mild acidic conditions to form methoxy enol ethers, which are stable under basic conditions and resist nucleophilic attack. This allows selective transformation of other functional groups in the molecule without affecting the carbonyl. After the desired reactions are complete, the protecting group can be removed easily using aqueous acid, regenerating the original carbonyl compound. Its volatility and reactivity make it suitable for use in anhydrous environments where controlled, reversible protection is needed. Also employed in the synthesis of fragrances and pharmaceuticals where precise functional group manipulation is critical.
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