2-(Phenylamino)benzamide

97%

Reagent Code: #226239
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CAS Number 1211-19-4

science Other reagents with same CAS 1211-19-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.25 g/mol
Formula C₁₃H₁₂N₂O
badge Registry Numbers
MDL Number MFCD00476529
thermostat Physical Properties
Boiling Point 413.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of dyes and pharmaceuticals. It serves as a building block for compounds with biological activity, including potential kinase inhibitors in medicinal chemistry. Also applied in the development of fluorescent materials and sensors due to its aromatic structure and ability to form stable complexes with metals. Its amide and aniline functional groups allow for easy modification in multi-step synthesis routes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,810.00
inventory 1g
10-20 days ฿9,530.00

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2-(Phenylamino)benzamide
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Used as an intermediate in organic synthesis, particularly in the production of dyes and pharmaceuticals. It serves as a building block for compounds with biological activity, including potential kinase inhibitors in medicinal chemistry. Also applied in the development of fluorescent materials and sensors due to its aromatic structure and ability to form stable complexes with metals. Its amide and aniline functional groups allow for easy modification in multi-step synthesis routes.

Used as an intermediate in organic synthesis, particularly in the production of dyes and pharmaceuticals. It serves as a building block for compounds with biological activity, including potential kinase inhibitors in medicinal chemistry. Also applied in the development of fluorescent materials and sensors due to its aromatic structure and ability to form stable complexes with metals. Its amide and aniline functional groups allow for easy modification in multi-step synthesis routes.

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