1608-93-1

Basic information

• Product Name: 5,5-diethyldihydrofuran-2(3H)-one
• CAS NO: 1608-93-1
• Molecular Formula: C₈H₁₄O₂
• Molecular Weight: 142.1956
• Mol File: 1608-93-1.mol
• Article Data: 18

Chemical Properties

• Boiling Point: 220.5°C at 760 mmHg
• Flash Point: 82.3°C
• Density: 0.949g/cm³
• Vapor Pressure: 0.112mmHg at 25°C
• Refractive Index: 1.43
• CAS DataBase Reference: 5,5-diethyldihydrofuran-2(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5,5-diethyldihydrofuran-2(3H)-one(1608-93-1)
• EPA Substance Registry System: 5,5-diethyldihydrofuran-2(3H)-one(1608-93-1)

Safety Data

• Hazardous Substances Data: 1608-93-1(Hazardous Substances Data)

Upstream product

• 1113-00-4 4-ethyl-hexane-1,4-diol 
• 60-29-7 diethyl ether 
• 543-20-4 succinoyl dichloride 
• 71-43-2 benzene 
• 108-30-5 succinic acid anhydride 
• 925-90-6 ethylmagnesium bromide 
• 584-02-1 2-pentanol 
• 292638-85-8 acrylic acid methyl ester 
• 74-96-4 ethyl bromide 
• 96-22-0 pentan-3-one 
• 121802-58-2 (Z)-3-Ethyl-6-(1-methoxymethyl-1H-imidazol-2-yl)-6-triisopropylsilanyloxy-hex-5-en-3-ol 
• 84786-96-9 1-(2-chloroethyl)-4-methyl-2,6,7-trioxabicyclo[2.2.2]octane 
• 107-94-8 chloropropionic acid 
• 140-88-5 ethyl acrylate 

Relevant articles and documents

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Scalable synthetic oligodeoxynucleotide purification with use of a catching by polymerization, washing, and releasing approach

Synthetic oligodeoxynucleotides are purified with use of a catching by polymerization, washing, and releasing approach. The method does not require any chromatography, and purification is achieved by simple operations such as shaking, washing, and extraction. It is therefore useful for large-scale purification of synthetic oligonucleotide drugs. In addition to purification of oligonucleotides, this catching by polymerization concept is expected to be equally useful for purification of other synthetic oligomers such as peptides and oligosaccharides.

A novel synthesis of γ,δ-unsaturated aldehydes from α-formyl-γ-lactones

A preparatively useful one-step transformation of γ,γ- disubstituted α-formyl-γ-lactones into trisubstituted γ,δ-unsaturated aldehydes is described, by means of catalytic amounts of either AcOH or AcOEt in the vapor phase over a glass support. A mechanistic rationale is proposed. Copyright

Synthesis of new furan derivatives and 4-hydroxy aldehydes from 4-hydroxy 1-enol ethers

Starting from 4-hydroxy 1-enol ethers 3 different γ-lactols 4 were successfully prepared by acidic hydrolysis. Subsequent oxidation of 4 with pyridinium chlorochromate (PCC) led to γ-lactones 6 in good to excellent overall yields. Treatment of γ-lactols 4