Identification | Back Directory | [Name]
5,6-dihydro-2H-pyran-3-carbaldehyde | [CAS]
13417-49-7 | [Synonyms]
EINECS 236-515-4 5,6-Dihydro-2H-pyran-3-carbaldehyde 5, 6-dihydro-2-H pyran-3-formaldehyde 2H-Pyran-3-carboxaldehyde, 5,6-dihydro- | [EINECS(EC#)]
236-515-4 | [Molecular Formula]
C6H8O2 | [MDL Number]
MFCD08146636 | [MOL File]
13417-49-7.mol | [Molecular Weight]
112.13 |
Chemical Properties | Back Directory | [Boiling point ]
49.2 °C | [density ]
1.114 g/cm3 | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [Appearance]
Colorless to light yellow Liquid | [InChI]
InChI=1S/C6H8O2/c7-4-6-2-1-3-8-5-6/h2,4H,1,3,5H2 | [InChIKey]
RKXCKEHBMLDWET-UHFFFAOYSA-N | [SMILES]
C1OCCC=C1C=O |
Hazard Information | Back Directory | [Uses]
5,6-Dihydro-2H-pyran-3-carboxaldehyde is a useful synthetic intermediate and a derivative of acrolein (A191200); a compound well-known for its use in the synthesis of acrylic acid. | [Synthesis]
Acrolein [stabilized] (40 g, 713 mmol) was dissolved in a solvent mixture of dichloromethane (105 mL) and deionized water (2.3 mL) at room temperature and stirred to form a homogeneous mixture. Phosphoric acid (12.7 mL) was slowly added dropwise to the above mixture. The reaction system was heated to reflux and the reaction was continued overnight. Upon completion of the reaction, the reaction mixture was purified by reduced pressure distillation (110-150 °C, 20 mmHg) to afford the target product 5,6-dihydro-2-H pyran-3-carbaldehyde (12.6 g, 15.7% yield). Mass spectrometry result (m/z): [M + H]+ 113.1. | [References]
[1] Monatshefte fuer Chemie, 1990, vol. 121, # 11, p. 963 - 970 [2] New Journal of Chemistry, 2008, vol. 32, # 8, p. 1354 - 1358 [3] Angewandte Chemie - International Edition, 2013, vol. 52, # 23, p. 6072 - 6075 [4] Angew. Chem., 2013, vol. 125, # 23, p. 6188 - 6191 [5] Patent: WO2016/85939, 2016, A2. Location in patent: Paragraph 00259 |
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