(1R,3AS,4E,7AR)-4-[(2Z)-2-[(5S)-5-[[(1,1-DIMETHYLETHYL)DIMETHYLSILYL]OXY]-2-METHYLENECYCLOHEXYLIDENE]ETHYLIDENE]OCTAHYDRO-7A-METHYL-1-[(1R,2E,4R)-1,4,5-TRIMETHYL-2-HEXEN-1-YL]-1H-INDENE

95%

Reagent Code: #232356
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CAS Number 104846-62-0

science Other reagents with same CAS 104846-62-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 510.92 g/mol
Formula C₃₄H₅₈OSi
badge Registry Numbers
MDL Number MFCD10574891
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in advanced organic synthesis, particularly in the development of complex natural products and pharmaceutical intermediates. Its intricate stereochemistry makes it valuable as a chiral building block for constructing biologically active molecules, especially in the synthesis of terpenoids and other polycyclic compounds. Commonly employed in research settings for stereoselective transformations, including cyclization and coupling reactions, to assemble structurally diverse frameworks with high precision.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿52,350.00
(1R,3AS,4E,7AR)-4-[(2Z)-2-[(5S)-5-[[(1,1-DIMETHYLETHYL)DIMETHYLSILYL]OXY]-2-METHYLENECYCLOHEXYLIDENE]ETHYLIDENE]OCTAHYDRO-7A-METHYL-1-[(1R,2E,4R)-1,4,5-TRIMETHYL-2-HEXEN-1-YL]-1H-INDENE
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Used in advanced organic synthesis, particularly in the development of complex natural products and pharmaceutical intermediates. Its intricate stereochemistry makes it valuable as a chiral building block for constructing biologically active molecules, especially in the synthesis of terpenoids and other polycyclic compounds. Commonly employed in research settings for stereoselective transformations, including cyclization and coupling reactions, to assemble structurally diverse frameworks with high precis

Used in advanced organic synthesis, particularly in the development of complex natural products and pharmaceutical intermediates. Its intricate stereochemistry makes it valuable as a chiral building block for constructing biologically active molecules, especially in the synthesis of terpenoids and other polycyclic compounds. Commonly employed in research settings for stereoselective transformations, including cyclization and coupling reactions, to assemble structurally diverse frameworks with high precision.

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