(4-Bromo-3,5-dimethylthiophen-2-yl)boronicacid

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Reagent Code: #154623
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CAS Number 172872-73-0

science Other reagents with same CAS 172872-73-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.91 g/mol
Formula C₆H₈BBrO₂S
badge Registry Numbers
MDL Number MFCD29078892
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry, Lightproof, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation with aryl or heteroaryl halides, facilitating the construction of biaryl structures. The bromo and methyl substituents on the thiophene ring enhance reactivity and influence electronic properties, making it valuable in the development of functional materials, such as organic semiconductors and conjugated polymers. Commonly employed in medicinal chemistry for building blocks in drug discovery due to the stability and modularity it offers in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿11,730.00
inventory 50mg
10-20 days ฿18,760.00
inventory 100mg
10-20 days ฿30,010.00
inventory 250mg
10-20 days ฿51,010.00

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(4-Bromo-3,5-dimethylthiophen-2-yl)boronicacid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation with aryl or heteroaryl halides, facilitating the construction of biaryl structures. The bromo and methyl substituents on the thiophene ring enhance reactivity and influence electronic properties, making it valuable in the development of functional materials, suc

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation with aryl or heteroaryl halides, facilitating the construction of biaryl structures. The bromo and methyl substituents on the thiophene ring enhance reactivity and influence electronic properties, making it valuable in the development of functional materials, such as organic semiconductors and conjugated polymers. Commonly employed in medicinal chemistry for building blocks in drug discovery due to the stability and modularity it offers in synthetic pathways.

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