trans-Methyl6-oxabicyclo[3.1.0]hexane-3-carboxylate

95%

Reagent Code: #214110
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CAS Number 86885-57-6

science Other reagents with same CAS 86885-57-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 142.15 g/mol
Formula C₇H₁₀O₃
badge Registry Numbers
MDL Number MFCD25541717
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as a chiral building block for pharmaceuticals and natural products. Its strained bicyclic structure makes it valuable in ring-opening reactions and cycloadditions to construct complex molecular frameworks. Commonly employed in the development of bioactive compounds, especially in medicinal chemistry research for designing enzyme inhibitors and neuroactive agents. Also serves as a versatile intermediate in asymmetric synthesis due to its stereochemical stability and functional group compatibility.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿46,970.00
trans-Methyl6-oxabicyclo[3.1.0]hexane-3-carboxylate
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Used in organic synthesis as a chiral building block for pharmaceuticals and natural products. Its strained bicyclic structure makes it valuable in ring-opening reactions and cycloadditions to construct complex molecular frameworks. Commonly employed in the development of bioactive compounds, especially in medicinal chemistry research for designing enzyme inhibitors and neuroactive agents. Also serves as a versatile intermediate in asymmetric synthesis due to its stereochemical stability and functional grou
Used in organic synthesis as a chiral building block for pharmaceuticals and natural products. Its strained bicyclic structure makes it valuable in ring-opening reactions and cycloadditions to construct complex molecular frameworks. Commonly employed in the development of bioactive compounds, especially in medicinal chemistry research for designing enzyme inhibitors and neuroactive agents. Also serves as a versatile intermediate in asymmetric synthesis due to its stereochemical stability and functional group compatibility.
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