2-(5-Bromo-4-methylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

98%

Reagent Code: #151446
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CAS Number 1111095-99-8

science Other reagents with same CAS 1111095-99-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 303.02 g/mol
Formula C₁₁H₁₆BBrO₂S
badge Registry Numbers
MDL Number MFCD12405479
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in pharmaceutical, agrochemical, and materials science research. The bromothiophene moiety allows further functionalization, enhancing its utility in developing conjugated systems for organic electronics and bioactive compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,840.00
250mg
10-20 days ฿4,820.00
1g
10-20 days ฿13,000.00
2-(5-Bromo-4-methylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in pharmaceutical, agrochemical, and materials science research. The bromothiophene moiety allows further functionalization, enhancing its utility in developing conjugated systems for organic electronics and bioactive compounds.

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in pharmaceutical, agrochemical, and materials science research. The bromothiophene moiety allows further functionalization, enhancing its utility in developing conjugated systems for organic electronics and bioactive compounds.

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