3-(Difluoromethoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine

98%

Reagent Code: #179957
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CAS Number 1188302-00-2

science Other reagents with same CAS 1188302-00-2

blur_circular Chemical Specifications

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Weight 286.08 g/mol
Formula C₁₂H₁₇BF₂N₂O₃
badge Registry Numbers
MDL Number MFCD18382479
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 biologically active pyridine derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical research and development, particularly in creating novel drug candidates targeting kinase inhibition and central nervous system disorders. The difluoromethoxy and amino functional groups enhance binding selectivity and metabolic stability in final compounds. Commonly employed in late-stage functionalization during medicinal chemistry optimization.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,460.00
inventory 250mg
10-20 days ฿35,190.00
inventory 1g
10-20 days ฿92,900.00

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3-(Difluoromethoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active pyridine derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical research and development, particularly in creating novel drug candidates targeting kinase inhibition and central nervous system disorders. The difluoromethoxy and amino functional groups enhance binding selectivity and metabolic stability in final compounds. Commonl

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active pyridine derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical research and development, particularly in creating novel drug candidates targeting kinase inhibition and central nervous system disorders. The difluoromethoxy and amino functional groups enhance binding selectivity and metabolic stability in final compounds. Commonly employed in late-stage functionalization during medicinal chemistry optimization.

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