62055-46-3

Basic information

• Product Name: 2-Propenal, 3-ethoxy-2-methyl-, (E)-
• Synonyms: (E)-3-ethoxy-2-methyl-prop-2-enal;3-Ethoxy-2-methylacrylaldehyde;2-Propenal,3-ethoxy-2-methyl-,(E);3-ETHOXY-2-METHYL-2-PROPEN-1-AL
• CAS NO: 62055-46-3
• Molecular Formula: C6H10O2
• Molecular Weight: 114.144
• Mol File: 62055-46-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 91-93 °C(Press: 19 Torr)
• Density: 0.9604 g/cm3
• CAS DataBase Reference: 2-Propenal, 3-ethoxy-2-methyl-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenal, 3-ethoxy-2-methyl-, (E)-(62055-46-3)
• EPA Substance Registry System: 2-Propenal, 3-ethoxy-2-methyl-, (E)-(62055-46-3)

Safety Data

• Hazardous Substances Data: 62055-46-3(Hazardous Substances Data)

Upstream product

• 928-55-2 ethyl 1-propenyl ether 

Downstream Products

• 85495-17-6 3-Methyl-benzo[4,5]imidazo[1,2-a]pyrimidine 
• 61578-00-5 6-methylpyrazolo[1,5-a]pyrimidine 
• 138254-44-1 6-Methylpyrazolo(1,5-a)pyrimidine-3-carbonitrile 
• 832741-06-7 ethyl 6-methylpyrazolo[1,5-a]pyrimidine-3-carboxylate 
• 1195782-42-3 5-methyl-2-oxo-1-(4-fluorophenyl)-1,2-dihydropyridine-3-carboxylic acid 
• 1303507-57-4 3-benzyl-3-ethyl-6-methyl-3H-[1,2]-oxathiolo[4,3-b]pyridine 1,1-dioxide 
• 1303507-55-2 3-benzyl-3-ethyl-4-[(E)-2-formylprop-1-enylamino]-5H-1,2-oxathiole 2,2-dioxide 
• 1303507-58-5 3,3-dibenzyl-6-methyl-3H-[1,2]-oxathiolo[4,3-b]pyridine 1,1-dioxide 
• 90905-61-6 (5-methylpyrimidin-2-yl)methanol 
• 226905-73-3 5-methyl-2-(4-trifluoromethylphenyl)pyrimidine 
• 129339-66-8 methyl 2-benzoylamino-5-ethoxy-4-methylpenta-2,4-dienoate 
• 129339-69-1 2-benzoylamino-5-ethoxy-4-methylpenta-2,4-dienoic acid 
• 155409-79-3 (+)-<(S)R>-1-Ethoxy-2-methyl-4-(p-tolylsulfinyl)-1,3-butadiene 
• 358726-34-8 (-)-2-methyl-3-[1-(S)-(2,4,6-triisopropylphenyl)ethoxy]prop-2-enal 

Relevant articles and documents

Direct formylation of enol ethers using cyanuric chloride and N,N-dimethylformamide

A new method to prepare α,β-unsaturated enol aldehydes is described. 3-Ethoxymethacrolein (1) and 5-formyl-3,4-dihydro-2H-pyran (5) were effectively prepared from enol ethers and the Vilsmeier-Haack type complex, derived from cyanuric chloride and DMF. One byproduct, amidine 4, was also characterized.