(±)-cis-Bicyclo[3.2.0]hept-2-en-6-one

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Reagent Code: #144827
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CAS Number 13173-09-6

science Other reagents with same CAS 13173-09-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 108.14 g/mol
Formula C₇H₈O
badge Registry Numbers
MDL Number MFCD06798168
thermostat Physical Properties
Boiling Point 158-160°C (Lit.)
inventory_2 Storage & Handling
Density 1.0260
Storage Room temperature, seal, dry

description Product Description

Used primarily as a key intermediate in the synthesis of prostaglandins, which are biologically active compounds involved in inflammation, blood flow, and reproductive processes. Its strained bicyclic structure and functional groups make it valuable in constructing complex organic molecules, especially in pharmaceutical research. Commonly employed in ring-opening and cycloaddition reactions to build chiral centers with high stereocontrol. Also utilized in academic and industrial settings for developing new synthetic methodologies and exploring reaction mechanisms in organic chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,090.00
inventory 5g
10-20 days ฿3,800.00
inventory 10g
10-20 days ฿7,590.00
inventory 100g
10-20 days ฿61,530.00
inventory 25g
10-20 days ฿17,700.00

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(±)-cis-Bicyclo[3.2.0]hept-2-en-6-one
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Used primarily as a key intermediate in the synthesis of prostaglandins, which are biologically active compounds involved in inflammation, blood flow, and reproductive processes. Its strained bicyclic structure and functional groups make it valuable in constructing complex organic molecules, especially in pharmaceutical research. Commonly employed in ring-opening and cycloaddition reactions to build chiral centers with high stereocontrol. Also utilized in academic and industrial settings for developing n

Used primarily as a key intermediate in the synthesis of prostaglandins, which are biologically active compounds involved in inflammation, blood flow, and reproductive processes. Its strained bicyclic structure and functional groups make it valuable in constructing complex organic molecules, especially in pharmaceutical research. Commonly employed in ring-opening and cycloaddition reactions to build chiral centers with high stereocontrol. Also utilized in academic and industrial settings for developing new synthetic methodologies and exploring reaction mechanisms in organic chemistry.

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