145127-34-0

Basic information

• Product Name: 2H-Pyran-4-ol, tetrahydro-4-(3-methylphenyl)-
• CAS NO: 145127-34-0
• Molecular Formula: C12H16O2
• Molecular Weight: 192.258
• Mol File: 145127-34-0.mol

Chemical Properties

• CAS DataBase Reference: 2H-Pyran-4-ol, tetrahydro-4-(3-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyran-4-ol, tetrahydro-4-(3-methylphenyl)-(145127-34-0)
• EPA Substance Registry System: 2H-Pyran-4-ol, tetrahydro-4-(3-methylphenyl)-(145127-34-0)

Safety Data

• Hazardous Substances Data: 145127-34-0(Hazardous Substances Data)

Upstream product

• 29943-42-8 Tetrahydro-4H-pyran-4-one 
• 28987-79-3 m-tolylmagnesium bromide 

Downstream Products

• 1289486-16-3 ethyl 3-(benzyloxy)-4-(3-(4-methoxytetrahydro-2H-pyran-4-yl)benzyloxy)benzoate 
• 1289486-15-2 4-(3-((2-(benzyloxy)-4-bromophenoxy)methyl)phenyl)-4-methoxytetrahydro-2H-pyran 
• 1289486-13-0 4-(3-((2-(benzyloxy)-4-chlorophenoxy)methyl)phenyl)-4-methoxytetrahydro-2H-pyran 
• 1289486-12-9 4-(3-((2-(benzyloxy)phenoxy)methyl)phenyl)-4-methoxytetrahydro-2H-pyran 
• 1289486-10-7 2-(benzyloxy)-N-(3-(4-methoxytetrahydro-2H-pyran-4-yl)benzyl)-5-nitroaniline 
• 1289486-08-3 2-(benzyloxy)-N-(3-(4-methoxytetrahydro-2H-pyran-4-yl)benzyl)-5-methylaniline 
• 1289486-06-1 2-(benzyloxy)-5-chloro-N-(3-(4-methoxytetrahydro-2H-pyran-4-yl)benzyl)aniline 
• 1289486-04-9 2-(benzyloxy)-4-chloro-N-(3-(4-methoxytetrahydro-2H-pyran-4-yl) benzyl) aniline 
• 1289486-03-8 2-(benzyloxy)-N-(3-(4-methoxytetrahydro-2H-pyran-4-yl) benzyl) aniline 
• 1289486-01-6 N-(2-(benzyloxy)-5-nitrophenyl)-N-(3-(4-methoxytetrahydro-2H-pyran-4-yl)benzyl)methanesulfonamide 
• 1289485-98-8 N-(2-(benzyloxy)-5-methylphenyl)-N-(3-(4-methoxytetrahydro-2H-pyran-4-yl)benzyl)methanesulfonamide 
• 1289485-97-7 N-(2-(benzyloxy)-5-chlorophenyl)-N-(3-(4-methoxytetrahydro-2H-pyran-4-yl)benzyl)methanesulfonamide 
• 1289485-95-5 N-(2-(benzyloxy)-4-chlorophenyl)-N-(3-(4-methoxytetrahydro-2H-pyran-4-yl)benzyl)methanesulfonamide 
• 1289485-93-3 N-(2-(benzyloxy)phenyl)-N-(3-(4-methoxytetrahydro-2H-pyran-4-yl)benzyl)methanesulfonamide 

Relevant articles and documents

Oxidative C–H alkynylation of 3,6-dihydro-2H-pyrans

Current synthesis of α-substituted 3,6-dihydro-2H-pyrans dominantly relies on functional group transformation. Herein, a direct and practical oxidative C–H alkynylation and alkenylation of 3,6-dihydro-2H-pyran skeletons with a range of potassium trifluoro