1014716-67-6

Basic information

• Product Name: 4-FC₆H₄B(OCH₂)2C(CH₃)CH₂OH
• Synonyms: 4-FC₆H₄B(OCH₂)2C(CH₃)CH₂OH
• CAS NO: 1014716-67-6
• Molecular Weight: 224.04
• Mol File: 1014716-67-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-FC₆H₄B(OCH₂)2C(CH₃)CH₂OH(CAS DataBase Reference)
• NIST Chemistry Reference: 4-FC₆H₄B(OCH₂)2C(CH₃)CH₂OH(1014716-67-6)
• EPA Substance Registry System: 4-FC₆H₄B(OCH₂)2C(CH₃)CH₂OH(1014716-67-6)

Safety Data

• Hazardous Substances Data: 1014716-67-6(Hazardous Substances Data)

Upstream product

• 77-85-0 2-(hydroxymethyl)-2-methylpropane-1,3-diol 
• 1765-93-1 4-fluoroboronic acid 

Downstream Products

• 58861-53-3 4-fluorophenylpyridine 
• 1352708-15-6 ((2-(4-fluorophenyl)-5-methyl-1,3,2-dioxaborinan-5-yl)methoxy)trimethylsilane 

Relevant articles and documents

Silyl-protected dioxaborinanes: Application in the Suzuki cross-coupling reaction

The synthesis of a range of novel silyl-protected dioxaborinanes as a column- and bench-stable boron reagent were found to be advantageous to achieving good yields in palladium-catalysed cross-coupling reactions under standard conditions. This journal is The Royal Society of Chemistry.

Cyclic triolborates: Air- and water-stable ate complexes of organoboronic acids

(Chemical Equation Presented) A borate in the hand is a convenient reagent for palladium- and copper-catalyzed C-C and C-N bond-forming reactions, especially when, like the title bench-stable complexes, it demonstrates high transmetalation efficiency. Cyclic triolborates can be synthesized readily from organoboronic acids (see scheme), can be handled and stored without special precautions, and are relatively soluble in organic solvents.