5-(2-Tolyl)thiophene-2-boronic acid

95%

Reagent Code: #92238
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CAS Number 2225181-05-3

science Other reagents with same CAS 2225181-05-3

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Weight 218.07984 g/mol
Formula C₁₁H₁₁BO₂S
inventory_2 Storage & Handling
Storage -20℃

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex organic compounds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in constructing carbon-carbon bonds. Also employed in the development of organic electronic materials, such as polymers and small molecules for OLEDs and organic semiconductors. Its stability and reactivity make it a versatile tool in medicinal chemistry for designing drug candidates.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿12,402.00
inventory 100mg
10-20 days ฿44,892.00

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5-(2-Tolyl)thiophene-2-boronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex organic compounds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in constructing carbon-carbon bonds. Also employed in the development of organic electronic materials, such as polymers and small molecules for OLEDs and organic semiconductors. Its stability

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex organic compounds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in constructing carbon-carbon bonds. Also employed in the development of organic electronic materials, such as polymers and small molecules for OLEDs and organic semiconductors. Its stability and reactivity make it a versatile tool in medicinal chemistry for designing drug candidates.

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