2-Amino-N-(2-bromophenyl)benzamide

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Reagent Code: #215795
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CAS Number 34489-85-5

science Other reagents with same CAS 34489-85-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.14 g/mol
Formula C₁₃H₁₁BrN₂O
badge Registry Numbers
MDL Number MFCD08443320
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. It serves as a building block for heterocyclic compounds like quinazolinones and benzodiazepines, which exhibit antimicrobial, anti-inflammatory, and anticancer properties. Its structure allows for easy functionalization, making it valuable in medicinal chemistry research and drug discovery. Also employed in the preparation of fluorescent dyes and sensors due to its amide and aromatic amine groups that contribute to electron delocalization and light emission properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,850.00
inventory 250mg
10-20 days ฿16,460.00

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2-Amino-N-(2-bromophenyl)benzamide
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. It serves as a building block for heterocyclic compounds like quinazolinones and benzodiazepines, which exhibit antimicrobial, anti-inflammatory, and anticancer properties. Its structure allows for easy functionalization, making it valuable in medicinal chemistry research and drug discovery. Also employed in the preparation of fluorescent dyes and sensors due to its amide and aro

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. It serves as a building block for heterocyclic compounds like quinazolinones and benzodiazepines, which exhibit antimicrobial, anti-inflammatory, and anticancer properties. Its structure allows for easy functionalization, making it valuable in medicinal chemistry research and drug discovery. Also employed in the preparation of fluorescent dyes and sensors due to its amide and aromatic amine groups that contribute to electron delocalization and light emission properties.

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