(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethanol

90%

Reagent Code: #230292
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CAS Number 1263166-90-0

science Other reagents with same CAS 1263166-90-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.22 g/mol
Formula C₁₀H₁₄O
badge Registry Numbers
MDL Number MFCD26142970
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used primarily as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceuticals and natural products. Its strained bicyclic structure and functional handle (hydroxyl group) make it valuable in ring-opening reactions and cycloadditions, enabling the construction of polycyclic frameworks. Commonly employed in the development of bioactive compounds, including potential antiviral and anticancer agents, due to its ability to mimic structural motifs found in biologically active molecules. Also utilized in materials science for designing rigid, three-dimensional scaffolds in molecular engineering.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10mg
10-20 days ฿3,800.00
50mg
10-20 days ฿5,500.00
250mg
10-20 days ฿13,110.00
1g
10-20 days ฿36,410.00
5g
10-20 days ฿115,090.00
(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethanol
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Used primarily as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceuticals and natural products. Its strained bicyclic structure and functional handle (hydroxyl group) make it valuable in ring-opening reactions and cycloadditions, enabling the construction of polycyclic frameworks. Commonly employed in the development of bioactive compounds, including potential antiviral and anticancer agents, due to its ability to mimic structural motifs found in biologically act

Used primarily as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceuticals and natural products. Its strained bicyclic structure and functional handle (hydroxyl group) make it valuable in ring-opening reactions and cycloadditions, enabling the construction of polycyclic frameworks. Commonly employed in the development of bioactive compounds, including potential antiviral and anticancer agents, due to its ability to mimic structural motifs found in biologically active molecules. Also utilized in materials science for designing rigid, three-dimensional scaffolds in molecular engineering.

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