Methyl2-amino-5-bromo-4-methylbenzoate

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Reagent Code: #213828
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CAS Number 1824597-08-1

science Other reagents with same CAS 1824597-08-1

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scatter_plot Molecular Information
Weight 244.09 g/mol
Formula C₉H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD23379700
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with central nervous system activity. It serves in the preparation of substituted benzodiazepines and other heterocyclic compounds due to the presence of both amino and ester functional groups, which allow for further chemical modifications. The bromo substituent enables cross-coupling reactions, making it valuable in medicinal chemistry for building complex drug molecules. Also employed in research settings for designing novel bioactive compounds and in the production of agrochemicals as a building block for herbicides and plant growth regulators.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,760.00
inventory 250mg
10-20 days ฿11,920.00
inventory 1g
10-20 days ฿38,630.00

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Methyl2-amino-5-bromo-4-methylbenzoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with central nervous system activity. It serves in the preparation of substituted benzodiazepines and other heterocyclic compounds due to the presence of both amino and ester functional groups, which allow for further chemical modifications. The bromo substituent enables cross-coupling reactions, making it valuable in medicinal chemistry for building complex drug mol

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with central nervous system activity. It serves in the preparation of substituted benzodiazepines and other heterocyclic compounds due to the presence of both amino and ester functional groups, which allow for further chemical modifications. The bromo substituent enables cross-coupling reactions, making it valuable in medicinal chemistry for building complex drug molecules. Also employed in research settings for designing novel bioactive compounds and in the production of agrochemicals as a building block for herbicides and plant growth regulators.

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