2,6-Diisopropylphenylimidoneophylidene molybdenum(VI) bis(hexafluoro-t-butoxide)

95%

Reagent Code: #178240
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CAS Number 139220-25-0

science Other reagents with same CAS 139220-25-0

blur_circular Chemical Specifications

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Weight 765.535 g/mol
Formula C₃₀H₃₅F₁₂MoNO₂
badge Registry Numbers
MDL Number MFCD00269857
inventory_2 Storage & Handling
Storage 2-8°C, argon-filled

description Product Description

Used as a highly active metathesis catalyst in organic synthesis, particularly in ring-closing metathesis (RCM) and cross-metathesis (CM) reactions. It enables the formation of carbon-carbon double bonds with excellent selectivity and functional group tolerance. Commonly applied in the synthesis of complex molecules such as pharmaceuticals, natural products, and advanced materials. Exhibits superior stability and reactivity compared to earlier generation catalysts, especially in sterically hindered and electron-deficient substrates. Often employed in low catalytic loadings under inert atmosphere conditions.

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inventory 50mg
10-20 days ฿23,450.00

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2,6-Diisopropylphenylimidoneophylidene molybdenum(VI) bis(hexafluoro-t-butoxide)
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Used as a highly active metathesis catalyst in organic synthesis, particularly in ring-closing metathesis (RCM) and cross-metathesis (CM) reactions. It enables the formation of carbon-carbon double bonds with excellent selectivity and functional group tolerance. Commonly applied in the synthesis of complex molecules such as pharmaceuticals, natural products, and advanced materials. Exhibits superior stability and reactivity compared to earlier generation catalysts, especially in sterically hindered and e

Used as a highly active metathesis catalyst in organic synthesis, particularly in ring-closing metathesis (RCM) and cross-metathesis (CM) reactions. It enables the formation of carbon-carbon double bonds with excellent selectivity and functional group tolerance. Commonly applied in the synthesis of complex molecules such as pharmaceuticals, natural products, and advanced materials. Exhibits superior stability and reactivity compared to earlier generation catalysts, especially in sterically hindered and electron-deficient substrates. Often employed in low catalytic loadings under inert atmosphere conditions.

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