3-Bromo-5-nitrobenzamide

≥95%

Reagent Code: #148363
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CAS Number 54321-80-1

science Other reagents with same CAS 54321-80-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.03 g/mol
Formula C₇H₅BrN₂O₃
badge Registry Numbers
MDL Number MFCD01529620
thermostat Physical Properties
Boiling Point 311.1°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure allows for further functionalization, making it valuable in medicinal chemistry for creating compounds with potential antitumor, antimicrobial, or anti-inflammatory activity. Commonly employed in organic synthesis to introduce the benzamide scaffold bearing electron-withdrawing groups, facilitating cross-coupling reactions and nucleophilic substitutions. Also utilized in the preparation of agrochemicals and specialty chemicals requiring specific substitution patterns on the aromatic ring.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,360.00
inventory 1g
10-20 days ฿4,700.00

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3-Bromo-5-nitrobenzamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure allows for further functionalization, making it valuable in medicinal chemistry for creating compounds with potential antitumor, antimicrobial, or anti-inflammatory activity. Commonly employed in organic synthesis to introduce the benzamide scaffold bearing electron-withdrawing groups, facilitating cross-coupling reactions and nucleophilic substitutions. A

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure allows for further functionalization, making it valuable in medicinal chemistry for creating compounds with potential antitumor, antimicrobial, or anti-inflammatory activity. Commonly employed in organic synthesis to introduce the benzamide scaffold bearing electron-withdrawing groups, facilitating cross-coupling reactions and nucleophilic substitutions. Also utilized in the preparation of agrochemicals and specialty chemicals requiring specific substitution patterns on the aromatic ring.

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