2-Bromo-N-methylacetamide

95%

Reagent Code: #149134
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CAS Number 34680-81-4

science Other reagents with same CAS 34680-81-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.9898 g/mol
Formula C₃H₆BrNO
badge Registry Numbers
MDL Number MFCD06800288
thermostat Physical Properties
Boiling Point 273.6 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for introducing bromoalkyl functional groups, enabling further chemical transformations such as alkylation and heterocycle formation. Commonly employed in the synthesis of N-containing compounds including alkaloids and bioactive molecules. Its reactivity makes it valuable in medicinal chemistry for constructing complex molecular frameworks.

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Test Parameter Specification
Appearance White to Off-White to Dark Yellow Solid or Liquid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿180.00
inventory 1g
10-20 days ฿560.00
inventory 5g
10-20 days ฿1,780.00
inventory 25g
10-20 days ฿7,100.00
inventory 100g
10-20 days ฿21,560.00

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2-Bromo-N-methylacetamide
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for introducing bromoalkyl functional groups, enabling further chemical transformations such as alkylation and heterocycle formation. Commonly employed in the synthesis of N-containing compounds including alkaloids and bioactive molecules. Its reactivity makes it valuable in medicinal chemistry for constructing complex molecular frameworks.

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for introducing bromoalkyl functional groups, enabling further chemical transformations such as alkylation and heterocycle formation. Commonly employed in the synthesis of N-containing compounds including alkaloids and bioactive molecules. Its reactivity makes it valuable in medicinal chemistry for constructing complex molecular frameworks.

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