2-[2-(Benzyloxy)ethyl]oxirane

95%

Reagent Code: #173452
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CAS Number 94426-72-9

science Other reagents with same CAS 94426-72-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.23 g/mol
Formula C₁₁H₁₄O₂
badge Registry Numbers
MDL Number MFCD27934088
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a reactive intermediate in organic synthesis, this compound serves as a versatile building block for introducing epoxy and ether functionalities into more complex molecules. Its epoxide ring readily undergoes acid- or base-catalyzed opening, enabling the formation of polyether structures or functionalized alcohols. It is particularly valuable in the preparation of specialty polymers, surfactants, and pharmaceuticals where a benzyloxy-terminated ethylene oxide spacer is required. The presence of the benzyl group allows for further modification or deprotection under mild conditions, making it useful in multi-step synthesis and protective group strategies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,000.00

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2-[2-(Benzyloxy)ethyl]oxirane
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Used primarily as a reactive intermediate in organic synthesis, this compound serves as a versatile building block for introducing epoxy and ether functionalities into more complex molecules. Its epoxide ring readily undergoes acid- or base-catalyzed opening, enabling the formation of polyether structures or functionalized alcohols. It is particularly valuable in the preparation of specialty polymers, surfactants, and pharmaceuticals where a benzyloxy-terminated ethylene oxide spacer is required. The pre

Used primarily as a reactive intermediate in organic synthesis, this compound serves as a versatile building block for introducing epoxy and ether functionalities into more complex molecules. Its epoxide ring readily undergoes acid- or base-catalyzed opening, enabling the formation of polyether structures or functionalized alcohols. It is particularly valuable in the preparation of specialty polymers, surfactants, and pharmaceuticals where a benzyloxy-terminated ethylene oxide spacer is required. The presence of the benzyl group allows for further modification or deprotection under mild conditions, making it useful in multi-step synthesis and protective group strategies.

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