3-Bromo-N-Methoxy-N-Methyl-Propionamide
95%
- Product Code: 150786
CAS:
128562-58-3
| Molecular Weight: | 196.04 g./mol | Molecular Formula: | C₅H₁₀BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20621450 | |
| Melting Point: | Boiling Point: | 187.5±42.0 °C(Predicted) | |
| Density: | 1.452±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature |
Product Description:
Used as a key reagent in organic synthesis, particularly in the preparation of ketones through the Weinreb–Nahm amide pathway. It reacts with organometallic reagents such as Grignard or organolithium compounds to provide stable intermediates that yield ketones selectively, avoiding over-addition and reducing the formation of by-products. Commonly employed in pharmaceutical synthesis where precise carbonyl construction is required. Its ability to control reactivity makes it valuable in multi-step synthesis of complex molecules, including natural products and active pharmaceutical ingredients.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $769.33 |
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| 0.250 | 10-20 days | $1,442.85 |
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| 1.000 | 10-20 days | $2,885.70 |
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3-Bromo-N-Methoxy-N-Methyl-Propionamide
Used as a key reagent in organic synthesis, particularly in the preparation of ketones through the Weinreb–Nahm amide pathway. It reacts with organometallic reagents such as Grignard or organolithium compounds to provide stable intermediates that yield ketones selectively, avoiding over-addition and reducing the formation of by-products. Commonly employed in pharmaceutical synthesis where precise carbonyl construction is required. Its ability to control reactivity makes it valuable in multi-step synthesis of complex molecules, including natural products and active pharmaceutical ingredients.
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