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

97%

Reagent Code: #138517
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CAS Number 22312-62-5

science Other reagents with same CAS 22312-62-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.28 g/mol
Formula C₁₄H₁₄N₂O
badge Registry Numbers
MDL Number MFCD00442835
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of heterocyclic compounds and pharmaceuticals. It serves as a building block in the development of kinase inhibitors and other biologically active molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its amide and amine functional groups, which facilitate molecular diversification. Also utilized in the synthesis of dyes and fluorescent probes for biochemical labeling. Its aromatic and polar characteristics make it suitable for solid-phase synthesis and combinatorial chemistry applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿970.00
inventory 1g
10-20 days ฿2,900.00
inventory 5g
10-20 days ฿13,550.00
inventory 25g
10-20 days ฿47,340.00

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2-Amino-N-(m-tolyl)benzamide
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Used as an intermediate in organic synthesis, particularly in the production of heterocyclic compounds and pharmaceuticals. It serves as a building block in the development of kinase inhibitors and other biologically active molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its amide and amine functional groups, which facilitate molecular diversification. Also utilized in the synthesis of dyes and fluorescent probes for biochemical labeling. Its a

Used as an intermediate in organic synthesis, particularly in the production of heterocyclic compounds and pharmaceuticals. It serves as a building block in the development of kinase inhibitors and other biologically active molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its amide and amine functional groups, which facilitate molecular diversification. Also utilized in the synthesis of dyes and fluorescent probes for biochemical labeling. Its aromatic and polar characteristics make it suitable for solid-phase synthesis and combinatorial chemistry applications.

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