106319-08-8

Basic information

• Product Name: 2H-Pyran-2-one,6-methyl-4-(1-methylethyl)-(9CI)
• Synonyms: 2H-Pyran-2-one,6-methyl-4-(1-methylethyl)-(9CI)
• CAS NO: 106319-08-8
• Molecular Formula: C9H12O2
• Molecular Weight: 152.19038
• Product Categories: ISOPROPYL
• Mol File: 106319-08-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2H-Pyran-2-one,6-methyl-4-(1-methylethyl)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyran-2-one,6-methyl-4-(1-methylethyl)-(9CI)(106319-08-8)
• EPA Substance Registry System: 2H-Pyran-2-one,6-methyl-4-(1-methylethyl)-(9CI)(106319-08-8)

Safety Data

• Hazardous Substances Data: 106319-08-8(Hazardous Substances Data)

Upstream product

• 675-10-5 4-hydroxy-6-methyl-2-pyron 
• 920-39-8 isopropylmagnesium bromide 
• 488788-59-6 6-methyl-2-pyrone-4-trifluoromethanesulfonate 
• 86310-03-4 (E)-2-methyl-5-methylthiohex-3-en-2-one 
• 87616-00-0 3-(1-methylethyl)-5-oxo-3-hexenoic acid 
• 150942-98-6 t-butyl lithioacetate 
• 113219-60-6 (E)-3-Hydroxy-3-isopropyl-5-methylsulfanyl-hex-4-enoic acid tert-butyl ester 
• 87615-98-3 1,1-dimethylethyl 3-(1-methylethyl)-5-oxo-3-hexenoate 
• 540-88-5 acetic acid tert-butyl ester 

Downstream Products

• 106319-17-9 4-(1-methylethyl)-6-(2-oxo-2-phenylethyl)-2H-pyran-2-one 
• 106319-16-8 6-(2-hydroxy-2-phenylethyl)-4-(1-methylethyl)-2H-pyran-2-one 

Relevant articles and documents

Formal ring-opening/cross-coupling reactions of 2-pyrones: Iron-catalyzed entry into stereodefined dienyl carboxylates

Open access: Despite the exceptional level of sophistication in cross-coupling chemistry, reactions of substrates that incorporate the leaving group as an integral part into a heterocyclic scaffold are scarce. The title reaction outlines the utility of this reaction format (see scheme; acac=acetylacetonate), provides a convenient entry into stereodefined diene carboxylates, and adds a new chapter to the field of iron catalysis. Copyright

A Versatile Synthesis of α-Pyrones

The α-oxoketene dithioacetal functionality is exploited in a versatile and efficient synthesis of annulated and simple α-pyrones.The alkyl substitution pattern about the α-pyrone ring can be modified at all four olefinic carbon atoms in a systematic manner.