(4S)-1-Methyl-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptane

95%

Reagent Code: #232544
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CAS Number 203719-53-3

science Other reagents with same CAS 203719-53-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.23 g/mol
Formula C₁₀H₁₆O
badge Registry Numbers
MDL Number MFCD00074837
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used in the synthesis of complex organic molecules, particularly in pharmaceuticals and natural products. Its strained bicyclic structure and ether functional group make it valuable as an intermediate in ring-opening and cycloaddition reactions. Commonly employed in the development of bioactive compounds due to its ability to mimic structural motifs found in terpenes and other biologically active molecules. Also utilized in asymmetric synthesis, where the chiral center at the 4-position allows for stereoselective transformations.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,600.00
inventory 25g
10-20 days ฿16,660.00
(4S)-1-Methyl-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptane
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Used in the synthesis of complex organic molecules, particularly in pharmaceuticals and natural products. Its strained bicyclic structure and ether functional group make it valuable as an intermediate in ring-opening and cycloaddition reactions. Commonly employed in the development of bioactive compounds due to its ability to mimic structural motifs found in terpenes and other biologically active molecules. Also utilized in asymmetric synthesis, where the chiral center at the 4-position allows for stereo

Used in the synthesis of complex organic molecules, particularly in pharmaceuticals and natural products. Its strained bicyclic structure and ether functional group make it valuable as an intermediate in ring-opening and cycloaddition reactions. Commonly employed in the development of bioactive compounds due to its ability to mimic structural motifs found in terpenes and other biologically active molecules. Also utilized in asymmetric synthesis, where the chiral center at the 4-position allows for stereoselective transformations.

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