2-Amino-N-(p-tolyl)benzamide

98%

Reagent Code: #215482
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CAS Number 32212-38-7

science Other reagents with same CAS 32212-38-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.27 g/mol
Formula C₁₄H₁₄N₂O
badge Registry Numbers
MDL Number MFCD00115975
thermostat Physical Properties
Melting Point 189 °C
Boiling Point 325.5±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.210±0.06 g/cm3(Predicted)
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. Also employed in research for designing enzyme inhibitors and receptor ligands. Its structure supports conjugation in fluorescent probes and sensors for biochemical assays.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,840.00
inventory 1g
10-20 days ฿3,540.00
inventory 5g
10-20 days ฿10,870.00
inventory 25g
10-20 days ฿34,240.00

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2-Amino-N-(p-tolyl)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. Also employed in research for designing enzyme inhibitors and receptor ligands. Its structure supports conjugation in fluorescent probes and sensors for biochemical assays.

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. Also employed in research for designing enzyme inhibitors and receptor ligands. Its structure supports conjugation in fluorescent probes and sensors for biochemical assays.

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