N-(5-Bromo-2-methoxyphenyl)acetamide

98%

Reagent Code: #219131
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CAS Number 88301-40-0

science Other reagents with same CAS 88301-40-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.09 g/mol
Formula C₉H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD12546479
thermostat Physical Properties
Melting Point 122 °C
Boiling Point 348.6±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.500±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of analgesic and anti-inflammatory agents. Its structure allows for further functionalization in heterocyclic synthesis, making it valuable in medicinal chemistry research. Commonly employed in the preparation of brominated aniline derivatives through hydrolysis or substitution reactions. Also utilized in the design of kinase inhibitors and other biologically active molecules due to the presence of bromine and electron-donating methoxy group, which influence binding affinity and selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,330.00
inventory 5g
10-20 days ฿27,550.00
inventory 1g
10-20 days ฿8,310.00

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N-(5-Bromo-2-methoxyphenyl)acetamide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of analgesic and anti-inflammatory agents. Its structure allows for further functionalization in heterocyclic synthesis, making it valuable in medicinal chemistry research. Commonly employed in the preparation of brominated aniline derivatives through hydrolysis or substitution reactions. Also utilized in the design of kinase inhibitors and other biologically active molecules due to the presence of bromi

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of analgesic and anti-inflammatory agents. Its structure allows for further functionalization in heterocyclic synthesis, making it valuable in medicinal chemistry research. Commonly employed in the preparation of brominated aniline derivatives through hydrolysis or substitution reactions. Also utilized in the design of kinase inhibitors and other biologically active molecules due to the presence of bromine and electron-donating methoxy group, which influence binding affinity and selectivity.

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