Iodo(triethyl phosphite)copper(I)

97%

Reagent Code: #200383
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CAS Number 51717-23-8

science Other reagents with same CAS 51717-23-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 356.61 g/mol
Formula C₆H₁₅CuIO₃P
badge Registry Numbers
MDL Number MFCD00074947
thermostat Physical Properties
Melting Point 110-116°C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a reagent in organic synthesis, particularly in conjugate addition reactions of organocopper compounds to α,β-unsaturated carbonyl compounds. It enables the formation of carbon-carbon bonds with high selectivity, especially in the synthesis of complex molecules such as natural products and pharmaceuticals. Its reactivity is milder compared to other organocopper reagents, allowing for better functional group tolerance. Commonly employed in the preparation of chiral intermediates when combined with asymmetric ligands. Also utilized in cross-coupling reactions under palladium-free conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿740.00
inventory 1g
10-20 days ฿2,560.00
inventory 5g
10-20 days ฿10,440.00
inventory 50g
10-20 days ฿73,140.00
inventory 25g
10-20 days ฿38,380.00
Iodo(triethyl phosphite)copper(I)
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Used as a reagent in organic synthesis, particularly in conjugate addition reactions of organocopper compounds to α,β-unsaturated carbonyl compounds. It enables the formation of carbon-carbon bonds with high selectivity, especially in the synthesis of complex molecules such as natural products and pharmaceuticals. Its reactivity is milder compared to other organocopper reagents, allowing for better functional group tolerance. Commonly employed in the preparation of chiral intermediates when combined with

Used as a reagent in organic synthesis, particularly in conjugate addition reactions of organocopper compounds to α,β-unsaturated carbonyl compounds. It enables the formation of carbon-carbon bonds with high selectivity, especially in the synthesis of complex molecules such as natural products and pharmaceuticals. Its reactivity is milder compared to other organocopper reagents, allowing for better functional group tolerance. Commonly employed in the preparation of chiral intermediates when combined with asymmetric ligands. Also utilized in cross-coupling reactions under palladium-free conditions.

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