2-(4-acetylanilino)-N-benzhydrylacetamide

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Reagent Code: #215473
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CAS Number 853693-74-0

science Other reagents with same CAS 853693-74-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 358.43 g/mol
Formula C₂₃H₂₂N₂O₂
thermostat Physical Properties
Boiling Point 635.8±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.179±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. Shows potential in the development of anti-inflammatory and analgesic agents due to structural similarity to known aniline-based inhibitors. Also investigated for use in central nervous system drug candidates, particularly those targeting neuropathic pain pathways. Its benzhydryl and acetanilide moieties contribute to membrane permeability, making it suitable for studies in blood-brain barrier penetration. Employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize lead compounds.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿18,350.00
inventory 50mg
10-20 days ฿24,910.00

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2-(4-acetylanilino)-N-benzhydrylacetamide
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Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. Shows potential in the development of anti-inflammatory and analgesic agents due to structural similarity to known aniline-based inhibitors. Also investigated for use in central nervous system drug candidates, particularly those targeting neuropathic pain pathways. Its benzhydryl and acetanilide moieties contribute to membrane permeability, making it suitable for studies in blood-brain barrier penetratio

Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. Shows potential in the development of anti-inflammatory and analgesic agents due to structural similarity to known aniline-based inhibitors. Also investigated for use in central nervous system drug candidates, particularly those targeting neuropathic pain pathways. Its benzhydryl and acetanilide moieties contribute to membrane permeability, making it suitable for studies in blood-brain barrier penetration. Employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize lead compounds.

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