Methyl 2-bromo-6-nitrobenzoate

98%

Reagent Code: #206607
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CAS Number 135484-76-3

science Other reagents with same CAS 135484-76-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.04 g/mol
Formula C₈H₆BrNO₄
thermostat Physical Properties
Boiling Point 306.4°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its functional groups—bromine and nitro—allow for further transformations such as cross-coupling reactions and nucleophilic substitutions. Commonly employed in the development of active ingredients in crop protection products and in the synthesis of substituted aromatic compounds for medicinal chemistry research. The ester group facilitates derivatization or hydrolysis to access carboxylic acid derivatives.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿890.00
inventory 250mg
10-20 days ฿2,050.00
inventory 1g
10-20 days ฿6,470.00
inventory 5g
10-20 days ฿25,070.00

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Methyl 2-bromo-6-nitrobenzoate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its functional groups—bromine and nitro—allow for further transformations such as cross-coupling reactions and nucleophilic substitutions. Commonly employed in the development of active ingredients in crop protection products and in the synthesis of substituted aromatic compounds for medicinal chemistry research. The ester group facilitates derivatization or hydrolysis to access carboxylic aci
Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its functional groups—bromine and nitro—allow for further transformations such as cross-coupling reactions and nucleophilic substitutions. Commonly employed in the development of active ingredients in crop protection products and in the synthesis of substituted aromatic compounds for medicinal chemistry research. The ester group facilitates derivatization or hydrolysis to access carboxylic acid derivatives.
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