(3AS,4S,5S,7R,8R,9S,9aR,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-vinyldecahydro-4,9a-propanocyclopenta[8]annulen-5-yl 2-((methylsulfonyl)oxy)acetate

97%

Reagent Code: #136904
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CAS Number 60924-38-1

science Other reagents with same CAS 60924-38-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 456.59 g/mol
Formula C₂₃H₃₆O₇S
badge Registry Numbers
MDL Number MFCD13194965
thermostat Physical Properties
Boiling Point 571.0±50.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used primarily as a synthetic intermediate in the preparation of complex natural product derivatives, particularly in the synthesis of bioactive terpenoids and steroidal analogs. Its functional groups, including the ester with mesylate moiety, hydroxyl, and vinyl groups, allow for selective modifications in multi-step organic syntheses. The mesylate serves as an excellent leaving group for nucleophilic substitutions, while the vinyl group enables further transformations such as epoxidation or dihydroxylation, making it valuable in medicinal chemistry for building molecular complexity. It is also employed in structure-activity relationship studies due to its rigid polycyclic framework, which mimics core structures found in biologically active compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,490.00
inventory 5g
10-20 days ฿4,550.00
inventory 10g
10-20 days ฿7,310.00

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(3AS,4S,5S,7R,8R,9S,9aR,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-vinyldecahydro-4,9a-propanocyclopenta[8]annulen-5-yl 2-((methylsulfonyl)oxy)acetate
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Used primarily as a synthetic intermediate in the preparation of complex natural product derivatives, particularly in the synthesis of bioactive terpenoids and steroidal analogs. Its functional groups, including the ester with mesylate moiety, hydroxyl, and vinyl groups, allow for selective modifications in multi-step organic syntheses. The mesylate serves as an excellent leaving group for nucleophilic substitutions, while the vinyl group enables further transformations such as epoxidation or dihydroxylatio
Used primarily as a synthetic intermediate in the preparation of complex natural product derivatives, particularly in the synthesis of bioactive terpenoids and steroidal analogs. Its functional groups, including the ester with mesylate moiety, hydroxyl, and vinyl groups, allow for selective modifications in multi-step organic syntheses. The mesylate serves as an excellent leaving group for nucleophilic substitutions, while the vinyl group enables further transformations such as epoxidation or dihydroxylation, making it valuable in medicinal chemistry for building molecular complexity. It is also employed in structure-activity relationship studies due to its rigid polycyclic framework, which mimics core structures found in biologically active compounds.
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