1-phenylvinyl methanesulfonate

≥90%

Reagent Code: #222552
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CAS Number 1093253-55-4

science Other reagents with same CAS 1093253-55-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.24 g/mol
Formula C₉H₁₀O₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry, light-proof

description Product Description

Used primarily as a reactive intermediate in organic synthesis, this compound serves as a vinylating agent in the preparation of styrene derivatives and other aromatic olefins. It participates in palladium-catalyzed coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical manufacturing. Its activated vinyl group allows for facile nucleophilic attack, making it useful in the synthesis of complex molecules where controlled olefin insertion is required. Additionally, it functions as a protecting group reagent for alcohols and phenols in multi-step synthesis due to its selective deprotection under mild conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,660.00
inventory 250mg
10-20 days ฿19,300.00
1-phenylvinyl methanesulfonate
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Used primarily as a reactive intermediate in organic synthesis, this compound serves as a vinylating agent in the preparation of styrene derivatives and other aromatic olefins. It participates in palladium-catalyzed coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical manufacturing. Its activated vinyl group allows for facile nucleophilic attack, making it useful in the synthesis of complex molecules where controlled olefin insertion is required. Additional

Used primarily as a reactive intermediate in organic synthesis, this compound serves as a vinylating agent in the preparation of styrene derivatives and other aromatic olefins. It participates in palladium-catalyzed coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical manufacturing. Its activated vinyl group allows for facile nucleophilic attack, making it useful in the synthesis of complex molecules where controlled olefin insertion is required. Additionally, it functions as a protecting group reagent for alcohols and phenols in multi-step synthesis due to its selective deprotection under mild conditions.

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