4-Bromomethyl-3-nitrobenzoic acid

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Reagent Code: #143632
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CAS Number 55715-03-2

science Other reagents with same CAS 55715-03-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.04 g/mol
Formula C₈H₆BrNO₄
badge Registry Numbers
MDL Number MFCD00216575
thermostat Physical Properties
Melting Point 127-130 °C(lit.)
Boiling Point 392°C
inventory_2 Storage & Handling
Density 1.814
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its functional groups—bromomethyl, nitro, and carboxylic acid—allow for sequential modifications, enabling the construction of complex molecules. The bromomethyl group is reactive toward nucleophiles, facilitating alkylation or substitution reactions, while the nitro group can be reduced to an amine for further derivatization. The carboxylic acid moiety permits amide bond formation or esterification, making it valuable in the development of active pharmaceutical ingredients (APIs) and functionalized aromatic compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿990.00
inventory 5g
10-20 days ฿4,190.00
inventory 25g
10-20 days ฿17,350.00
inventory 10g
10-20 days ฿7,600.00

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4-Bromomethyl-3-nitrobenzoic acid
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its functional groups—bromomethyl, nitro, and carboxylic acid—allow for sequential modifications, enabling the construction of complex molecules. The bromomethyl group is reactive toward nucleophiles, facilitating alkylation or substitution reactions, while the nitro group can be reduced to an amine for further derivatization. The carboxylic acid moiety permits amide bond formation or ester

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its functional groups—bromomethyl, nitro, and carboxylic acid—allow for sequential modifications, enabling the construction of complex molecules. The bromomethyl group is reactive toward nucleophiles, facilitating alkylation or substitution reactions, while the nitro group can be reduced to an amine for further derivatization. The carboxylic acid moiety permits amide bond formation or esterification, making it valuable in the development of active pharmaceutical ingredients (APIs) and functionalized aromatic compounds.

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