5-Amino-2-methylbenzamide

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Reagent Code: #139095
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CAS Number 515131-52-9

science Other reagents with same CAS 515131-52-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.18 g/mol
Formula C₈H₁₀N₂O
badge Registry Numbers
MDL Number MFCD14618179
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting inflammation and central nervous system disorders. It serves as a building block in the preparation of heterocyclic compounds due to the presence of both amine and amide functional groups, enabling diverse chemical transformations. Commonly employed in research settings for designing novel compounds with potential biological activity. Also utilized in the manufacture of agrochemicals and dyes where substituted benzamides are required. Its structural features make it suitable for use in peptide coupling reactions and in the formation of Schiff bases for further derivatization.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,610.00
inventory 250mg
10-20 days ฿6,130.00
inventory 1g
10-20 days ฿20,280.00

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5-Amino-2-methylbenzamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting inflammation and central nervous system disorders. It serves as a building block in the preparation of heterocyclic compounds due to the presence of both amine and amide functional groups, enabling diverse chemical transformations. Commonly employed in research settings for designing novel compounds with potential biological activity. Also utilized i

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting inflammation and central nervous system disorders. It serves as a building block in the preparation of heterocyclic compounds due to the presence of both amine and amide functional groups, enabling diverse chemical transformations. Commonly employed in research settings for designing novel compounds with potential biological activity. Also utilized in the manufacture of agrochemicals and dyes where substituted benzamides are required. Its structural features make it suitable for use in peptide coupling reactions and in the formation of Schiff bases for further derivatization.

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