2-Amino-N-(2-chlorophenyl)benzamide

95%

Reagent Code: #138665
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CAS Number 838-77-7

science Other reagents with same CAS 838-77-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.7 g/mol
Formula C₁₃H₁₁ClN₂O
badge Registry Numbers
MDL Number MFCD00748574
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block in the preparation of heterocyclic compounds due to the presence of both amine and amide functional groups, which allow for cyclization reactions. Commonly employed in research settings for the design of novel bioactive molecules and in medicinal chemistry for structure-activity relationship studies. Also utilized in the production of dyes and pigments where aromatic amide structures contribute to color stability and lightfastness.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,200.00
inventory 250mg
10-20 days ฿2,690.00
inventory 1g
10-20 days ฿8,050.00

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2-Amino-N-(2-chlorophenyl)benzamide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block in the preparation of heterocyclic compounds due to the presence of both amine and amide functional groups, which allow for cyclization reactions. Commonly employed in research settings for the design of novel bioactive molecules and in medicinal chemistry for structure-activity relationship studies. Also utilized in the production

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block in the preparation of heterocyclic compounds due to the presence of both amine and amide functional groups, which allow for cyclization reactions. Commonly employed in research settings for the design of novel bioactive molecules and in medicinal chemistry for structure-activity relationship studies. Also utilized in the production of dyes and pigments where aromatic amide structures contribute to color stability and lightfastness.

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