57651-41-9

Basic information

• Product Name: 2-Furancarboxylic acid, tetrahydro-2-methyl-5-oxo-
• CAS NO: 57651-41-9
• Molecular Formula: C6H8O4
• Molecular Weight: 144.127
• Mol File: 57651-41-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-Furancarboxylic acid, tetrahydro-2-methyl-5-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Furancarboxylic acid, tetrahydro-2-methyl-5-oxo-(57651-41-9)
• EPA Substance Registry System: 2-Furancarboxylic acid, tetrahydro-2-methyl-5-oxo-(57651-41-9)

Safety Data

• Hazardous Substances Data: 57651-41-9(Hazardous Substances Data)

Upstream product

• 80-71-7 2-hydroxy-3-methylcyclopent-2-en-1-one 
• 855902-75-9 2-hydroxy-2,6-dimethyl-hept-5-enoic acid 
• 10028-15-6 ozone 
• 64-19-7 acetic acid 
• 56-23-5 tetrachloromethane 
• 3123-97-5 dihydro-5,5-dimethyl-2(3H)-furanone 
• 7697-37-2 nitric acid 

Downstream Products

• 93176-19-3 methyl 2-benzoyloxy-2-methyl-5-oxo-4-phenylselenopentanoate 
• 93221-32-0 methyl (S)-5-acetoxy-2-benzoyloxy-2-methylpentanoate 
• 83206-02-4 methyl 5-acetoxy-2-benzoyloxy-2-methylpentanoate 
• 93221-36-4 (S)-(3E,5E)-methyl 2-benzoyloxy-2-methyl-3,5-octadienoate 
• 83206-06-8 (3E,5E)-methyl 2-benzoyloxy-2-methyl-3,5-octadienoate 
• 93221-33-1 methyl (S)-2-benzoyloxy-5-hydroxy-2-methylpentanoate 
• 83206-03-5 methyl 2-benzoyloxy-5-hydroxy-2-methylpentanoate 
• 93221-35-3 (3E)-methyl (S)-2-benzoyloxy-2-methyl-5-oxo-3-pentenoate 
• 83206-05-7 (3E)-methyl 2-benzoyloxy-2-methyl-5-oxo-3-pentenoate 
• 93221-34-2 methyl (S)-2-benzoyloxy-2-methyl-5-oxopentanoate 
• 83206-04-6 methyl 2-benzoyloxy-2-methyl-5-oxopentanoate 
• 58801-71-1 gregatin B 
• 123-76-2 levulinic acid 
• 110-15-6 succinic acid 

Relevant articles and documents

Aerobic cascade oxidation of substituted cyclopentane-1,2-diones using metalloporphyrin catalysts

A method for the aerobic cascade oxidation of cyclopentane-1,2-diones using metal porphyrins as catalysts, yielding hydroxydiacids 2, ketoacid 3 and diketoacids 4 which are the intermediates of important biologically active compounds is reported. This method is operationally simple and can be employed under ambient conditions.