4,4,5,5-tetramethyl-2-3-[(methylsulfanyl)methyl]phenyl-1,3,2-dioxaborolane

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Reagent Code: #244503
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CAS Number 1414923-65-1

science Other reagents with same CAS 1414923-65-1

blur_circular Chemical Specifications

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Weight 264.19 g/mol
Formula C₁₄H₂₁BO₂S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its boron-containing structure allows it to react with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical, agrochemical, and materials science research. The methylsulfanyl group enhances reactivity and can act as a directing or modulating group in complex molecule assembly. Stable under standard conditions and compatible with various functional groups, it supports efficient and selective transformations in late-stage synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,100.00
inventory 1g
10-20 days ฿77,370.00
inventory 250mg
10-20 days ฿25,210.00

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4,4,5,5-tetramethyl-2-3-[(methylsulfanyl)methyl]phenyl-1,3,2-dioxaborolane
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Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its boron-containing structure allows it to react with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical, agrochemical, and materials science research. The methylsulfanyl group enhances reactivity and can act as a directing or modulating group in complex molecule assembly. Stable under standard conditions and compatible wit

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its boron-containing structure allows it to react with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical, agrochemical, and materials science research. The methylsulfanyl group enhances reactivity and can act as a directing or modulating group in complex molecule assembly. Stable under standard conditions and compatible with various functional groups, it supports efficient and selective transformations in late-stage synthesis.

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