N-(2-Aminoethyl)-2-hydroxybenzamide

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Reagent Code: #219082
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CAS Number 36288-93-4

science Other reagents with same CAS 36288-93-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.20 g/mol
Formula C₉H₁₂N₂O₂
badge Registry Numbers
MDL Number MFCD09735200
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly those targeting neurological and inflammatory pathways. Its structure supports the development of enzyme inhibitors due to the presence of both amide and amine functional groups, which can interact with biological targets. Also explored in the design of metal chelators for potential use in treating metal-related disorders. Additionally, it serves as a building block in the preparation of fluorescent probes for biochemical assays, leveraging the hydroxyl group for conjugation to fluorophores.

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inventory 1g
10-20 days ฿26,390.00

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N-(2-Aminoethyl)-2-hydroxybenzamide
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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly those targeting neurological and inflammatory pathways. Its structure supports the development of enzyme inhibitors due to the presence of both amide and amine functional groups, which can interact with biological targets. Also explored in the design of metal chelators for potential use in treating metal-related disorders. Additionally, it serves as a building block in the preparation of fluorescen

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly those targeting neurological and inflammatory pathways. Its structure supports the development of enzyme inhibitors due to the presence of both amide and amine functional groups, which can interact with biological targets. Also explored in the design of metal chelators for potential use in treating metal-related disorders. Additionally, it serves as a building block in the preparation of fluorescent probes for biochemical assays, leveraging the hydroxyl group for conjugation to fluorophores.

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