2-Amino-N-methyl-N-phenylbenzamide

95%

Reagent Code: #138631
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CAS Number 6632-37-7

science Other reagents with same CAS 6632-37-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.28 g/mol
Formula C₁₄H₁₄N₂O
badge Registry Numbers
MDL Number MFCD00443942
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block in the preparation of compounds with potential central nervous system activity. Also employed in the creation of dyes and pigments due to its aromatic and amide structure, contributing to lightfastness and stability. Additionally, it finds use in research settings for developing novel heterocyclic compounds through cyclization reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,010.00
inventory 1g
10-20 days ฿6,020.00
inventory 5g
10-20 days ฿28,080.00

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2-Amino-N-methyl-N-phenylbenzamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block in the preparation of compounds with potential central nervous system activity. Also employed in the creation of dyes and pigments due to its aromatic and amide structure, contributing to lightfastness and stability. Additionally, it finds use in research settings for developing novel heterocyclic compounds through cyclization reactions.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block in the preparation of compounds with potential central nervous system activity. Also employed in the creation of dyes and pigments due to its aromatic and amide structure, contributing to lightfastness and stability. Additionally, it finds use in research settings for developing novel heterocyclic compounds through cyclization reactions.

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