1,4-Epoxy-1,4-dihydronaphthalene

98%

Reagent Code: #181803
label
Alias 1,4-dihydrogen-1,4-epoxynaphthalene
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CAS Number 573-57-9

science Other reagents with same CAS 573-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 144.17 g/mol
Formula C₁₀H₈O
badge Registry Numbers
MDL Number MFCD00167584
thermostat Physical Properties
Melting Point 54-56 °C(lit.)
Boiling Point 241℃
inventory_2 Storage & Handling
Density 1.207
Storage Room temperature

description Product Description

Used as a reactive intermediate in organic synthesis, particularly in the preparation of naphthalene-based derivatives for pharmaceuticals and fine chemicals. Its strained epoxide ring undergoes ring-opening reactions with nucleophiles, enabling the introduction of functional groups at specific positions on the aromatic system. Commonly employed in the development of dyes, fluorescent probes, and polymer modifiers due to its ability to participate in cycloaddition and coupling reactions. Also serves as a building block in the synthesis of polycyclic compounds for materials science applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,170.00
inventory 5g
10-20 days ฿18,050.00
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1,4-Epoxy-1,4-dihydronaphthalene
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Used as a reactive intermediate in organic synthesis, particularly in the preparation of naphthalene-based derivatives for pharmaceuticals and fine chemicals. Its strained epoxide ring undergoes ring-opening reactions with nucleophiles, enabling the introduction of functional groups at specific positions on the aromatic system. Commonly employed in the development of dyes, fluorescent probes, and polymer modifiers due to its ability to participate in cycloaddition and coupling reactions. Also serves as a

Used as a reactive intermediate in organic synthesis, particularly in the preparation of naphthalene-based derivatives for pharmaceuticals and fine chemicals. Its strained epoxide ring undergoes ring-opening reactions with nucleophiles, enabling the introduction of functional groups at specific positions on the aromatic system. Commonly employed in the development of dyes, fluorescent probes, and polymer modifiers due to its ability to participate in cycloaddition and coupling reactions. Also serves as a building block in the synthesis of polycyclic compounds for materials science applications.

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