3-Bromo-N-Methoxy-N-Methyl-Propionamide

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Reagent Code: #150786
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CAS Number 128562-58-3

science Other reagents with same CAS 128562-58-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.04 g/mol
Formula C₅H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD20621450
thermostat Physical Properties
Boiling Point 187.5±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.452±0.06 g/cm3(Predicted)
Storage Room temperature

description 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.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,220.00
inventory 250mg
10-20 days ฿30,420.00
inventory 1g
10-20 days ฿60,840.00

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3-Bromo-N-Methoxy-N-Methyl-Propionamide
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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 synthesi

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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