(6E,10E,14E,18E)-2,3-EPOXY-2,6,10,15,19,23-EPOXY-2,6,10,15,19,23-HEXAMETHYL-6,10,14,18,22-TETRACOSAPENTAENE

90%

Reagent Code: #184052
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CAS Number 7200-26-2

science Other reagents with same CAS 7200-26-2

blur_circular Chemical Specifications

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Weight 426.72 g/mol
Formula C₃₀H₅₀O
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used in advanced organic synthesis as a specialized epoxidation reagent, particularly in the construction of complex polyene structures found in natural products and bioactive molecules. Its conjugated pentaene system with multiple epoxy groups allows for selective ring-opening reactions, enabling the formation of stereodefined oxygen-containing functional groups in pharmaceuticals and agrochemicals. It serves as a building block in the synthesis of terpenoids and other polycyclic compounds where precise control over stereochemistry and chain length is critical. Due to its sensitivity and reactivity, it is handled under inert conditions and primarily employed in research settings for developing novel synthetic pathways.

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inventory 1mg
10-20 days ฿34,210.00

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(6E,10E,14E,18E)-2,3-EPOXY-2,6,10,15,19,23-EPOXY-2,6,10,15,19,23-HEXAMETHYL-6,10,14,18,22-TETRACOSAPENTAENE
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Used in advanced organic synthesis as a specialized epoxidation reagent, particularly in the construction of complex polyene structures found in natural products and bioactive molecules. Its conjugated pentaene system with multiple epoxy groups allows for selective ring-opening reactions, enabling the formation of stereodefined oxygen-containing functional groups in pharmaceuticals and agrochemicals. It serves as a building block in the synthesis of terpenoids and other polycyclic compounds where precise

Used in advanced organic synthesis as a specialized epoxidation reagent, particularly in the construction of complex polyene structures found in natural products and bioactive molecules. Its conjugated pentaene system with multiple epoxy groups allows for selective ring-opening reactions, enabling the formation of stereodefined oxygen-containing functional groups in pharmaceuticals and agrochemicals. It serves as a building block in the synthesis of terpenoids and other polycyclic compounds where precise control over stereochemistry and chain length is critical. Due to its sensitivity and reactivity, it is handled under inert conditions and primarily employed in research settings for developing novel synthetic pathways.

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