2-Benzyloxirane

98%

Reagent Code: #149669
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CAS Number 4436-24-2

science Other reagents with same CAS 4436-24-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 134.18 g/mol
Formula C₉H₁₀O
badge Registry Numbers
MDL Number MFCD00074964
thermostat Physical Properties
Boiling Point 98-100  °C at 17 mmHg (lit.)
inventory_2 Storage & Handling
Density 1.02 g/mL at 25 °C (lit.)
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of beta-blockers and other pharmaceuticals. It reacts selectively with nucleophiles due to the strained epoxide ring, allowing for the introduction of functionalized side chains. Commonly employed in the synthesis of chiral compounds through asymmetric ring-opening reactions. Also utilized in the production of fine chemicals and agrochemicals where a benzyloxy-substituted ethanol framework is required. Its reactivity makes it valuable in laboratory-scale synthesis and medicinal chemistry research.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless to Yellow Liquid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,470.00
inventory 1g
10-20 days ฿3,920.00
inventory 5g
10-20 days ฿18,580.00
2-Benzyloxirane
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Used as an intermediate in organic synthesis, particularly in the preparation of beta-blockers and other pharmaceuticals. It reacts selectively with nucleophiles due to the strained epoxide ring, allowing for the introduction of functionalized side chains. Commonly employed in the synthesis of chiral compounds through asymmetric ring-opening reactions. Also utilized in the production of fine chemicals and agrochemicals where a benzyloxy-substituted ethanol framework is required. Its reactivity makes it v

Used as an intermediate in organic synthesis, particularly in the preparation of beta-blockers and other pharmaceuticals. It reacts selectively with nucleophiles due to the strained epoxide ring, allowing for the introduction of functionalized side chains. Commonly employed in the synthesis of chiral compounds through asymmetric ring-opening reactions. Also utilized in the production of fine chemicals and agrochemicals where a benzyloxy-substituted ethanol framework is required. Its reactivity makes it valuable in laboratory-scale synthesis and medicinal chemistry research.

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