2-(2-Bromo-3-methylphenyl)acetamide

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Reagent Code: #152950
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CAS Number 1824058-64-1

science Other reagents with same CAS 1824058-64-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.09 g/mol
Formula C₉H₁₀BrNO
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of bioactive molecules, particularly in the development of compounds with potential anti-inflammatory and analgesic properties. Its bromo-substituted aromatic structure allows for cross-coupling reactions, enabling the introduction of various functional groups during drug discovery processes. Also utilized in the synthesis of heterocyclic compounds due to its reactive amide and aryl bromide functionalities.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,340.00
inventory 250mg
10-20 days ฿5,200.00
inventory 1g
10-20 days ฿13,310.00
inventory 5g
10-20 days ฿52,150.00

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2-(2-Bromo-3-methylphenyl)acetamide
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Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of bioactive molecules, particularly in the development of compounds with potential anti-inflammatory and analgesic properties. Its bromo-substituted aromatic structure allows for cross-coupling reactions, enabling the introduction of various functional groups during drug discovery processes. Also utilized in the synthesis of heterocyclic compounds due to its reactive amide an

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of bioactive molecules, particularly in the development of compounds with potential anti-inflammatory and analgesic properties. Its bromo-substituted aromatic structure allows for cross-coupling reactions, enabling the introduction of various functional groups during drug discovery processes. Also utilized in the synthesis of heterocyclic compounds due to its reactive amide and aryl bromide functionalities.

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