
N-Butylphthalimide | CAS:1515-72-6
N-Butylphthalimide
- 名称:N-正丁基邻苯二甲酰亚胺; N-丁基酞酰亚胺 | N-Butylphthalimide
- CAS号:1515-72-6
- 别名:2-Butyl-1H-isoindole-1,3-(2H)-dione; N-(n-Butyl)phthalimide
- 分子式:C12H13NO2
- 分子量:203.24
- EINESC号:216-157-5
产品描述
物理化学性质
熔点 | 29-33 ºC |
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安全说明书 | S24/25 |
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Noyori, R. et al. Journal of the American Chemical Society, 106(22), 6709-6709 (1984)
Molecular design of a chiral Lewis acid for the asymmetric Claisen rearrangement.Maruoka, K. et al. Journal of the American Chemical Society, 117(3), 1165-1165 (1995)
Catalytic asymmetric oxidation of sulfides to sulfoxides with tert-butyl hydroperoxide using binaphthol as a chiral auxiliary.Komatsu N, et al. The Journal of Organic Chemistry, 58, 4529-4529 (1993)
New chiral binaphthalene-derived iminium salt organocatalysts for asymmetric epoxidation of alkenes.Philip C Bulman Page et al.The Journal of organic chemistry, 72(12), 4424-4430 (2007-05-18)
Evaluation of co-solvent fraction, pressure and temperature effects in analytical and preparative supercritical fluid chromatography.Dennis Åsberg et al.Journal of chromatography. A, 1374, 254-260 (2014-12-17)
Catalytic asymmetric epoxidation with (Salen) manganese (III) complex bearing binaphthyl groups of axial chirality.Sasaki, H. et al. Synlett, 1993(04), 300-300 (1993)
Asymmetric aza-Diels-Alder reaction catalyzed by boron reagent: Effect of biphenol and binaphthol ligand.Hattori, K. Yamamoto, H. Synlett, 1993(02), 129-129 (1993)
Asymmetric Diels-Alder reactions catalyzed by chiral lanthanide (III) trifluoromethanesulfonates. Unique structure of the triflate and stereoselective synthesis of both enantiomers using a single chiral source and a choice of achiral ligands.S. Kobayashi et al. Tetrahedron, 50(40), 11623-11623 (1994)
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Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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