N,N-Dimethyl-N-(methylsulfanylmethylene)ammonium Iodide

98%

Reagent Code: #217651
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CAS Number 29085-13-0

science Other reagents with same CAS 29085-13-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.1 g/mol
Formula C₄H₁₀INS
badge Registry Numbers
MDL Number MFCD17015287
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a reagent in organic synthesis, particularly in methylenation reactions where a carbonyl group is converted to a methylene group. It serves as a sulfur ylide precursor, enabling the formation of carbon-carbon double bonds under mild conditions. Commonly applied in the synthesis of alkenes from aldehydes and ketones, especially in complex molecule construction such as natural products and pharmaceuticals. Its iodide counterion enhances solubility in polar solvents, facilitating reaction efficiency in various synthetic pathways.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,740.00
5g
10-20 days ฿5,300.00
N,N-Dimethyl-N-(methylsulfanylmethylene)ammonium Iodide
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Used as a reagent in organic synthesis, particularly in methylenation reactions where a carbonyl group is converted to a methylene group. It serves as a sulfur ylide precursor, enabling the formation of carbon-carbon double bonds under mild conditions. Commonly applied in the synthesis of alkenes from aldehydes and ketones, especially in complex molecule construction such as natural products and pharmaceuticals. Its iodide counterion enhances solubility in polar solvents, facilitating reaction efficiency

Used as a reagent in organic synthesis, particularly in methylenation reactions where a carbonyl group is converted to a methylene group. It serves as a sulfur ylide precursor, enabling the formation of carbon-carbon double bonds under mild conditions. Commonly applied in the synthesis of alkenes from aldehydes and ketones, especially in complex molecule construction such as natural products and pharmaceuticals. Its iodide counterion enhances solubility in polar solvents, facilitating reaction efficiency in various synthetic pathways.

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