3-甲基戊醛
3-甲基戊醛 | |
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英文名 | 3-methylpentanal |
识别 | |
CAS号 | 15877-57-3 1730-94-5(3S) 51468-48-5(3R) |
性质 | |
化学式 | C6H12O |
摩尔质量 | 100.16 g·mol−1 |
沸点 | 122 °C(395 K)[1] |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
3-甲基戊醛是一种有机化合物,化学式为C6H12O,它存在S型和R型两种异构。它可由3-甲基戊醇经马丁试剂或吡啶氯铬酸盐氧化得到。[2][3]它可以被氧化为3-甲基戊酸。[4]
参考文献
- ^ Levene, P. A.; Rothen, Alexandre; Kuna, Martin. Optical rotation of configurationally related aldehydes. Journal of Biological Chemistry, 1935. 111: 739-747.
- ^ Saskia Thurnhofer, Walter Vetter. Synthesis of (S)-(+)-enantiomers of food-relevant (n-5)-monoenoic and saturated anteiso-fatty acids by a Wittig reaction. Tetrahedron. 2007-01, 63 (5): 1140–1145 [2022-03-07]. doi:10.1016/j.tet.2006.11.059. (原始内容存档于2018-07-01) (英语).
- ^ Zelong Lim, Peter J. Duggan, Soo San Wan, Guillaume Lessene, Adam G. Meyer, Kellie L. Tuck. Exploiting the Biginelli reaction: nitrogen-rich pyrimidine-based tercyclic α-helix mimetics. Tetrahedron. 2016-03, 72 (9): 1151–1160 [2022-03-07]. doi:10.1016/j.tet.2015.12.044. (原始内容存档于2020-02-19) (英语).
- ^ Panek (编). Category 3, Compounds with Four and Three Carbon Heteroatom Bonds: Three Carbon—Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Stuttgart: Georg Thieme Verlag. 2006 [2022-03-07]. ISBN 9783131187116. doi:10.1055/sos-sd-020-00065. (原始内容存档于2021-05-06) (英语).