7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyridine

CAS: 3319-15-1

Ref. 3D-DAA31915

Produktinformation

• Name: 7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyridine
• Synonyme: (1R)-1-(4-methoxyphenyl)ethanol, (4-Methoxyphenyl)methylcarbinol, (±)-1-(4-Methoxyphenyl)-1-ethanol, (±)-1-(p-Methoxyphenyl)ethanol, 1-(4-Methoxyphenyl)Ethanol, 1-(4-Methoxyphenyl)ethan-1-ol, 1-(p-Anisyl)ethanol, 1-Hydroxyethyl-4-methoxybenzene, 4-Methoxy-α-methylbenzenemethanol, 4-Methoxy-α-methylbenzyl alcohol, 4-Methoxyphenyl methyl carbinol, ALPHA-Methyl-p-anisyl alcohol, Benzenemethanol, 4-methoxy-α-methyl-, Benzyl alcohol, p-methoxy-α-methyl-, NSC 406712, p-Anisyl alcohol, α-methyl-, p-Methoxy-α-methylbenzyl alcohol, p-Methoxy-α-phenylethanol, p-Methoxyphenyl methyl carbinol, α-Methyl-4-methoxybenzenemethanol, α-Methyl-4-methoxybenzyl alcohol

Beschreibung

7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyridine is a primary alcohol that can be synthesized from alpha-methylbenzyl alcohol and styrene. The compound has been shown to be an excellent substrate for the aerobic photooxidation of the cell membrane. 7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyridine is also stereoselective and can be used as a chiral building block for enantiomerically pure polymers. It has been shown to have cationic polymerization properties. This compound is also capable of photooxidation of isoprene.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 152.19 g/mol
• Formel: C₉H₁₂O₂
• Reinheit: Min. 95%