(E)-8-Methoxy-2-((naphthalen-1-yloxy)methyl)-8-oxooct-2-enoic acid

98%

Reagent Code: #184817
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CAS Number 936221-69-1

science Other reagents with same CAS 936221-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 342.39 g/mol
Formula C₂₀H₂₂O₅
badge Registry Numbers
MDL Number MFCD28404586
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a synthetic intermediate for developing anti-inflammatory and anticancer agents. Shows potential in inhibiting specific enzymes involved in tumor growth and cellular proliferation. Also utilized in the study of structure-activity relationships for α,β-unsaturated carbonyl systems due to its conjugated double bond and methoxy substitution. Its naphthalene-based structure enhances lipophilicity, improving cell membrane permeability in drug design. Investigated for use in photodynamic therapy owing to its light-sensitive properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,790.00
inventory 250mg
10-20 days ฿17,990.00
inventory 1g
10-20 days ฿44,990.00

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(E)-8-Methoxy-2-((naphthalen-1-yloxy)methyl)-8-oxooct-2-enoic acid
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Used in pharmaceutical research as a synthetic intermediate for developing anti-inflammatory and anticancer agents. Shows potential in inhibiting specific enzymes involved in tumor growth and cellular proliferation. Also utilized in the study of structure-activity relationships for α,β-unsaturated carbonyl systems due to its conjugated double bond and methoxy substitution. Its naphthalene-based structure enhances lipophilicity, improving cell membrane permeability in drug design. Investigated for use in

Used in pharmaceutical research as a synthetic intermediate for developing anti-inflammatory and anticancer agents. Shows potential in inhibiting specific enzymes involved in tumor growth and cellular proliferation. Also utilized in the study of structure-activity relationships for α,β-unsaturated carbonyl systems due to its conjugated double bond and methoxy substitution. Its naphthalene-based structure enhances lipophilicity, improving cell membrane permeability in drug design. Investigated for use in photodynamic therapy owing to its light-sensitive properties.

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