1025351-09-0

Basic information

• Product Name: C₁₆H₁₂N₂O₂
• Synonyms: C₁₆H₁₂N₂O₂
• CAS NO: 1025351-09-0
• Molecular Weight: 264.283
• Mol File: 1025351-09-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₁₆H₁₂N₂O₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₆H₁₂N₂O₂(1025351-09-0)
• EPA Substance Registry System: C₁₆H₁₂N₂O₂(1025351-09-0)

Safety Data

• Hazardous Substances Data: 1025351-09-0(Hazardous Substances Data)

Upstream product

• 7251-61-8 2-methylquinoxaline 
• 100-51-6 benzyl alcohol 
• 100-52-7 benzaldehyde 
• 1448-87-9 2-chloroquinoxaline 
• 14135-39-8 [(benzoyloxy)methyl]zinc iodide 

Downstream Products

• 41242-94-8 2-hydroxymethylquinoxaline 

Relevant articles and documents

Synthesis of benzyl esters from the commercially available alcohols catalyzed by TBAI via C(sp3)-H bond functionalization

A direct esterification of alcohols catalyzed by TBAI via C(sp3)-H bond functionalization was achieved under mild and clean conditions. A series of benzyl esters were obtained in good to excellent yields via the C(sp3)-H bond functionalization of alkyl-substituted azaarenes.

Hydroxymethylations of aryl halides by Pd-catalyzed cross-couplings with (benzoyloxy)methylzinc iodide - Scope and limitations of the reaction

Palladium-catalyzed cross-coupling reactions of (benzoyloxymethyl)zinc iodide with diverse (het)aryl halides leading to (benzoyloxymethyl)(het)arenes were studied to define the scope of this reaction. It has been found that this reaction is only applicable for electron-deficient aryl halides and the most efficient it is for 2-halopyridines and 4-halopyrimidines. Deprotection of the intermediates gives (hydroxymethyl)pyridines and -pyrimidines in high yields. Georg Thieme Verlag Stuttgart.