N-(3,4-dimethylphenyl)-1-oxo-1H-isochromene-3-carboxamide

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Reagent Code: #245659
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CAS Number 354999-94-3

science Other reagents with same CAS 354999-94-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.32 g/mol
Formula C₁₈H₁₅NO₃
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and anticancer compounds. Its structural framework supports activity in enzyme inhibition, especially in targeting kinases involved in cellular signaling pathways. Also employed in research settings for structure-activity relationship (SAR) studies due to its ability to interact with biological receptors through hydrogen bonding and hydrophobic interactions. Additionally, it serves as a building block in the preparation of bioactive heterocyclic derivatives for drug discovery programs.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿8,790.00
inventory 25mg
10-20 days ฿17,590.00

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N-(3,4-dimethylphenyl)-1-oxo-1H-isochromene-3-carboxamide
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and anticancer compounds. Its structural framework supports activity in enzyme inhibition, especially in targeting kinases involved in cellular signaling pathways. Also employed in research settings for structure-activity relationship (SAR) studies due to its ability to interact with biological receptors through hydrogen bonding and hydrophobic interactions. Additionally, it serves a

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and anticancer compounds. Its structural framework supports activity in enzyme inhibition, especially in targeting kinases involved in cellular signaling pathways. Also employed in research settings for structure-activity relationship (SAR) studies due to its ability to interact with biological receptors through hydrogen bonding and hydrophobic interactions. Additionally, it serves as a building block in the preparation of bioactive heterocyclic derivatives for drug discovery programs.

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