1-(Benzyloxy)naphthalene

95%

Reagent Code: #148236
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CAS Number 607-58-9

science Other reagents with same CAS 607-58-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.29 g/mol
Formula C₁₇H₁₄O
badge Registry Numbers
MDL Number MFCD00078325
thermostat Physical Properties
Boiling Point 388.1°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a protecting group for hydroxyl functionalities during multi-step syntheses due to its stability under various reaction conditions. Also employed in the development of liquid crystals and optoelectronic materials because of its aromatic structure and electron-donating properties. Its derivative nature makes it valuable in constructing complex molecular architectures in medicinal chemistry research.

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Test Parameter Specification
Appearance Light yellow to yellow powder or crystals
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,910.00
inventory 250mg
10-20 days ฿3,220.00
inventory 1g
10-20 days ฿8,740.00

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1-(Benzyloxy)naphthalene
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a protecting group for hydroxyl functionalities during multi-step syntheses due to its stability under various reaction conditions. Also employed in the development of liquid crystals and optoelectronic materials because of its aromatic structure and electron-donating properties. Its derivative nature makes it valuable in constructing complex molecular architectures in medicin

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a protecting group for hydroxyl functionalities during multi-step syntheses due to its stability under various reaction conditions. Also employed in the development of liquid crystals and optoelectronic materials because of its aromatic structure and electron-donating properties. Its derivative nature makes it valuable in constructing complex molecular architectures in medicinal chemistry research.

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