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NUCIFERINE is , while it's Molecular Formula is C19H21NO2. The lotus leaf alkaloid has the effect of weight loss and lipid reduction, and can be used for content determination/identification/pharmacological experiments.
The CAS number of NUCIFERINE is 475-83-2.
More information of NUCIFERINE 475-83-2 are:
Synonyms |
4H-Dibenzo[de,g]quinoline,5,6,6a,7-tetrahydro-1,2-dimethoxy-6-methyl-, (R)-;6ab-Aporphine, 1,2-dimethoxy- (8CI);Nuciferine (6CI,7CI);(-)-Nuciferine;(R)-1,2-Dimethoxyaporphine;(R)-Nuciferine;1,2-Dimethoxy-6ab-aporphine;D-(-)-Nuciferine;Nuciferin;Sanjoinine E;l-Nuciferine; |
CAS Number |
475-83-2 |
Molecular Formula |
C19H21NO2 |
Molecular Weight |
295.381 |
Density |
1.15 g/cm3 |
Melting Point |
165.5°C |
Boiling Point |
430.7 °C at 760 mmHg |
Flash Point |
151.9 °C |
HS CODE |
29389090 |
PSA |
21.70000 |
LogP |
3.39380 |
Pka |
7.87±0.20(Predicted) |
Nuciferine is an aporphine alkaloid from Nelumbo lutea, the ba~e yields colourless crystals when crystallized from EtOH. It is laevorotatory, the following specific rotations having been recorded; [α] 22D- 157.5° and - 215°. The ultraviolet spectrum has three absorption maxima at 230, 272 and 310 mp. Two methoxyl groups and one methylimino group are present and the alkaloid may be characterized as the hydrochloride, m.p. 241°C (in vacuo) and the methiodide, m.p. 177-8°C. The optically inactive base has been synthesized and has m.p. 136-7°C, giving a hydrochloride in the form of small colourless prisms from H20, m.p. 258°C (dec.).
InChI:InChI=1/C19H21NO2/c1-20-9-8-13-11-16(21-2)19(22-3)18-14-7-5-4-6-12(14)10-15(20)17(13)18/h4-7,11,15H,8-10H2,1-3H3
Articles related to NUCIFERINE:
Article |
Source |
Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry |
Casagrande, Gleison A.,Deflon, Victor M.,Martins, Gabriel R.,Oliveira-Silva, Diogo,Perecim, Givago P.,Pinto, Leandro M. C.,Raminelli, Cristiano , (2020/08/13) |
Aporphine alkaloid synthesis and diversification via direct arylation |
Lafrance, Marc,Blaquiere, Nicole,Fagnou, Keith , p. 811 - 825 (2008/02/12) |
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