157007-74-4

Basic information

• Product Name: 3-Furancarboxylic acid, tetrahydro-2,2-dimethyl-5-oxo-, (3S)-
• CAS NO: 157007-74-4
• Molecular Formula: C7H10O4
• Molecular Weight: 158.154
• Mol File: 157007-74-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Furancarboxylic acid, tetrahydro-2,2-dimethyl-5-oxo-, (3S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Furancarboxylic acid, tetrahydro-2,2-dimethyl-5-oxo-, (3S)-(157007-74-4)
• EPA Substance Registry System: 3-Furancarboxylic acid, tetrahydro-2,2-dimethyl-5-oxo-, (3S)-(157007-74-4)

Safety Data

• Hazardous Substances Data: 157007-74-4(Hazardous Substances Data)

Upstream product

• 78597-75-8 (4S,5R)-4-(2-hydroxypropan-2-yl)-5-((-)-menthyloxy)-dihydrofuran-2(3H)-one 
• 156905-61-2 (S)-4-[1,3]Dioxolan-2-yl-5,5-dimethyl-dihydro-furan-2-one 
• 34566-25-1 ethyl 2,2-dimethyl-5-oxotetrahydro-3-furancarboxylate 
• 6934-77-6 β-carbomethoxy-γ,γ-dimethyl-γ-butyrolactone 
• 1187-70-8 (S)-2-isopropylsuccinic acid 
• 498-15-7 (+)-Δ³-carene 
• 7664-93-9 sulfuric acid 
• 67-66-3 chloroform 
• 10028-15-6 ozone 
• 100052-76-4 (S)-6,6-dimethyl-5-(2-methyl-propenyl)-tetrahydro-pyran-2-one 
• 27373-86-0 (R)-5,5-dimethyl-4-(3-methyl-but-1-en-c-yl)-dihydro-furan-2-one 
• 64-18-6 formic acid 
• 124744-28-1 ((R)-3,3-Dimethyl-oxiranyl)-acetic acid methyl ester 
• 79-91-4 terebic acid 

Relevant articles and documents

Highly diastereoselective addition of photochemically generated radicals to (5R)-(-)-menthyloxy-2[5H]-furanone - Synthesis of (-)-terebic acid

Photochemically generated ketyl and 2-dioxolanyl radicals are added with high diastereoselectivity (de > 95%) to (5R)-(-)-5-menthyloxy-2[5H]-furanone. This reaction is used for the asymmetric synthesis of (-)-terebic acid. The double bond is attacked by t

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KINETIC RESOLUTION OF RACEMIC β,γ-EPOXY ESTERS WITH PIG LIVER ESTERASE (PLE, E.C. 3.1.1.1.)

The β,γ-epoxy esters (+/-)-2 to (+/-)-6 were synthetisized.The E-values of kinetic resolution of 2, 3, 4, and 6 with PLE and the absolute configuration of the products of the hydrolysis were determined by the conversion to known compounds.