Methyl 3-amino-4-bromo-2-nitrobenzoate

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Reagent Code: #209161
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CAS Number 1207175-60-7

science Other reagents with same CAS 1207175-60-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.06 g/mol
Formula C₈H₇BrN₂O₄
badge Registry Numbers
MDL Number MFCD13677167
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed from light

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require substituted benzoate scaffolds. Its functional groups—amino, bromo, and nitro—allow for sequential transformations, such as coupling reactions, reductions, and nucleophilic substitutions, making it valuable in constructing complex organic molecules. Commonly employed in research settings for the preparation of dyes, fluorescent probes, and heterocyclic compounds. The presence of the ester group facilitates further derivatization, including hydrolysis or amidation, to fine-tune solubility and reactivity in final products.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿980.00
inventory 250mg
10-20 days ฿1,710.00
inventory 1g
10-20 days ฿4,950.00
inventory 5g
10-20 days ฿24,700.00
inventory 10g
10-20 days ฿49,380.00

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Methyl 3-amino-4-bromo-2-nitrobenzoate
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require substituted benzoate scaffolds. Its functional groups—amino, bromo, and nitro—allow for sequential transformations, such as coupling reactions, reductions, and nucleophilic substitutions, making it valuable in constructing complex organic molecules. Commonly employed in research settings for the preparation of dyes, fluorescent probes, and heterocyclic compoun

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require substituted benzoate scaffolds. Its functional groups—amino, bromo, and nitro—allow for sequential transformations, such as coupling reactions, reductions, and nucleophilic substitutions, making it valuable in constructing complex organic molecules. Commonly employed in research settings for the preparation of dyes, fluorescent probes, and heterocyclic compounds. The presence of the ester group facilitates further derivatization, including hydrolysis or amidation, to fine-tune solubility and reactivity in final products.

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