1-(Benzyloxy)-3-chlorobenzene

97%

Reagent Code: #154689
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CAS Number 24318-02-3

science Other reagents with same CAS 24318-02-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.68 g/mol
Formula C₁₃H₁₁ClO
badge Registry Numbers
MDL Number MFCD05863215
thermostat Physical Properties
Melting Point 59 °C
Boiling Point 321.1±17.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.175±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of substituted benzene derivatives for drug development, particularly in creating compounds with central nervous system activity. Also employed in the production of liquid crystals and organic electronic materials due to its stable aromatic structure and functional reactivity. Its chloro and ether groups allow for further chemical modifications through cross-coupling and nucleophilic substitution reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,330.00
inventory 250mg
10-20 days ฿8,950.00
inventory 1g
10-20 days ฿24,080.00

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1-(Benzyloxy)-3-chlorobenzene
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of substituted benzene derivatives for drug development, particularly in creating compounds with central nervous system activity. Also employed in the production of liquid crystals and organic electronic materials due to its stable aromatic structure and functional reactivity. Its chloro and ether groups allow for further chemical modifications through cross-coupling and nucleophilic substitution r

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of substituted benzene derivatives for drug development, particularly in creating compounds with central nervous system activity. Also employed in the production of liquid crystals and organic electronic materials due to its stable aromatic structure and functional reactivity. Its chloro and ether groups allow for further chemical modifications through cross-coupling and nucleophilic substitution reactions.

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