3-Bromo-N-methoxy-N-methylpicolinamide

≥95%

Reagent Code: #150518
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CAS Number 867353-49-9

science Other reagents with same CAS 867353-49-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.07 g/mol
Formula C₈H₉BrN₂O₂
badge Registry Numbers
MDL Number MFCD11975703
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as a key reagent in organic synthesis, particularly in the formation of ketones through the Weinreb–Nahm amide pathway. It reacts with organometallic reagents like Grignard or organolithium compounds to provide controlled addition products without over-addition, making it ideal for constructing complex molecules in pharmaceutical and natural product synthesis. Its stability and selectivity enhance efficiency in multi-step reactions, especially in the development of active pharmaceutical ingredients (APIs). Commonly employed in research laboratories and industrial settings for carbonyl elongation and functional group transformations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,980.00
inventory 1g
10-20 days ฿23,940.00

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3-Bromo-N-methoxy-N-methylpicolinamide
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Used as a key reagent in organic synthesis, particularly in the formation of ketones through the Weinreb–Nahm amide pathway. It reacts with organometallic reagents like Grignard or organolithium compounds to provide controlled addition products without over-addition, making it ideal for constructing complex molecules in pharmaceutical and natural product synthesis. Its stability and selectivity enhance efficiency in multi-step reactions, especially in the development of active pharmaceutical ingredients

Used as a key reagent in organic synthesis, particularly in the formation of ketones through the Weinreb–Nahm amide pathway. It reacts with organometallic reagents like Grignard or organolithium compounds to provide controlled addition products without over-addition, making it ideal for constructing complex molecules in pharmaceutical and natural product synthesis. Its stability and selectivity enhance efficiency in multi-step reactions, especially in the development of active pharmaceutical ingredients (APIs). Commonly employed in research laboratories and industrial settings for carbonyl elongation and functional group transformations.

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