Samarium(II) iodide

99.99%

Reagent Code: #235791
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CAS Number 32248-43-4

science Other reagents with same CAS 32248-43-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 404.17 g/mol
Formula SmI₂
badge Registry Numbers
MDL Number MFCD00058873
inventory_2 Storage & Handling
Density 0.922 g/mL at 25 °C
Storage Room temperature

description Product Description

Widely used in organic synthesis as a powerful reducing agent, especially in carbon-carbon bond-forming reactions. It promotes reductive couplings of carbonyl compounds, such as in the pinacol coupling reaction. It is also employed in the selective reduction of functional groups including sulfoxides, epoxides, and halides. Its ability to mediate Barbier-type reactions under mild conditions makes it valuable for constructing complex organic frameworks. Additionally, it serves as a single-electron transfer agent in cascade and cyclization reactions, enabling efficient synthesis of cyclic and polycyclic structures.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿28,000.00
inventory 5g
10-20 days ฿88,000.00
inventory 10g
10-20 days ฿150,000.00

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Samarium(II) iodide
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Widely used in organic synthesis as a powerful reducing agent, especially in carbon-carbon bond-forming reactions. It promotes reductive couplings of carbonyl compounds, such as in the pinacol coupling reaction. It is also employed in the selective reduction of functional groups including sulfoxides, epoxides, and halides. Its ability to mediate Barbier-type reactions under mild conditions makes it valuable for constructing complex organic frameworks. Additionally, it serves as a single-electron transfer

Widely used in organic synthesis as a powerful reducing agent, especially in carbon-carbon bond-forming reactions. It promotes reductive couplings of carbonyl compounds, such as in the pinacol coupling reaction. It is also employed in the selective reduction of functional groups including sulfoxides, epoxides, and halides. Its ability to mediate Barbier-type reactions under mild conditions makes it valuable for constructing complex organic frameworks. Additionally, it serves as a single-electron transfer agent in cascade and cyclization reactions, enabling efficient synthesis of cyclic and polycyclic structures.

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