2,5-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline

95%

Reagent Code: #176152
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CAS Number 939807-75-7

science Other reagents with same CAS 939807-75-7

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scatter_plot Molecular Information
Weight 255.0687464 g/mol
Formula C₁₂H₁₆BF₂NO₂
badge Registry Numbers
MDL Number MFCD09743045
inventory_2 Storage & Handling
Storage 2-8°C

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 industries. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of active pharmaceutical ingredients (APIs) and functional materials. The presence of fluoro substituents enhances reactivity and influences electronic properties, which can improve the metabolic stability and bioavailability of target compounds. Commonly employed in research and process chemistry for building fluorinated aromatic scaffolds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,800.00
inventory 250mg
10-20 days ฿18,030.00
inventory 5g
10-20 days ฿115,200.00
inventory 1g
10-20 days ฿40,000.00

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2,5-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
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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 industries. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of active pharmaceutical ingredients (APIs) and functional materials. The presence of fluoro substituents enhances reactivity and influences electronic properties, which can improve the metabolic st

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of active pharmaceutical ingredients (APIs) and functional materials. The presence of fluoro substituents enhances reactivity and influences electronic properties, which can improve the metabolic stability and bioavailability of target compounds. Commonly employed in research and process chemistry for building fluorinated aromatic scaffolds.

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