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2,6-Dimethylpiperidine | CAS:504-03-0
2,6-Dimethylpiperidine
  • Name:2,6-Dimethylpiperidine
  • CAS:504-03-0
  • Synonyms:2,6-Lupetidine
  • Molecular Formula:C7H15N
  • Molecular Weight:113.20
  • EINESC:207-981-6

Description

Properties

Water Solubility MISCIBLE
Boiling point 127-128 ºC
Flash point 11 ºC
Density 0.84
Refractive index 1.4384-1.4404

Safety

Symbol(GHS) F;C
Hazard Codes R11;R34
SDS/MSDS S16;S26;S36/37/39

SDS

Source SDS/MSDS Samples
没有数据没有数据
Synthetic Route
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Articles
Peer-Reviewed Papers
Density functional theory study of the FT-IR spectra of phthalimide and N-bromophthalimide.V Krishnakumar et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 62(4-5), 918-925 (2005-06-14) N-bromoimide/DBU combination as a new strategy for intermolecular allylic amination.Ying Wei et al.Organic letters, 15(20), 5186-5189 (2013-10-10) C2-symmetric cyclic selenium-catalyzed enantioselective bromoaminocyclization.Feng Chen et al.Journal of the American Chemical Society, 135(4), 1232-1235 (2013-01-15) Titrimetric determination of acetylenic hyponotics using organic brominating agents.A el-Brashy et al.Pharmaceutisch weekblad. Scientific edition, 10(2), 90-92 (1988-04-22) Titrimetric determination of para-aminobenzoic acid using N-bromophthalimide and N-bromosaccharin.K G Kumar et al.Journal of pharmaceutical and biomedical analysis, 7(5), 627-631 (1989-01-01) Colorimetric and titrimetric assay of isoniazid.A M el-Brashy et al.Journal of pharmaceutical and biomedical analysis, 10(6), 421-426 (1992-06-01) Titrimetric methods for the determination of some sulpha drugs using N-bromophthalimide and N-bromosaccharin.K G Kumar et al.The Analyst, 113(9), 1369-1372 (1988-09-01) Site-selective bromination of vancomycin.Tejas P Pathak et al.Journal of the American Chemical Society, 134(14), 6120-6123 (2012-04-03) Enantioselective synthesis of multisubstituted biaryl skeleton by chiral phosphoric acid catalyzed desymmetrization/kinetic resolution sequence.Keiji Mori et al.Journal of the American Chemical Society, 135(10), 3964-3970 (2013-02-19)
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