Methyl 3-amino-5-bromo-4-methoxybenzoate

95%

Reagent Code: #130502
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CAS Number 40258-74-0

science Other reagents with same CAS 40258-74-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.08 g/mol
Formula C₉H₁₀BrNO₃
badge Registry Numbers
MDL Number MFCD16039459
thermostat Physical Properties
Boiling Point 367.4±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.531±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—amino, bromo, and ester—allow for selective modifications, enabling the construction of complex heterocyclic structures. Commonly employed in coupling reactions and cyclization processes to form benzoxazole or benzimidazole derivatives with potential therapeutic activity. Also utilized in agrochemical research for designing novel pesticides due to its electron-withdrawing substituents and structural stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,540.00
inventory 250mg
10-20 days ฿14,540.00

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Methyl 3-amino-5-bromo-4-methoxybenzoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—amino, bromo, and ester—allow for selective modifications, enabling the construction of complex heterocyclic structures. Commonly employed in coupling reactions and cyclization processes to form benzoxazole or benzimidazole derivatives with potential therapeutic activity. Also utilized in agrochemical research

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—amino, bromo, and ester—allow for selective modifications, enabling the construction of complex heterocyclic structures. Commonly employed in coupling reactions and cyclization processes to form benzoxazole or benzimidazole derivatives with potential therapeutic activity. Also utilized in agrochemical research for designing novel pesticides due to its electron-withdrawing substituents and structural stability.

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