16-epi-isositsirikine manufacturers
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| | 16-epi-isositsirikine Basic information |
| Product Name: | 16-epi-isositsirikine | | Synonyms: | 16-epi-isositsirikine;(16R,19E)-19,20-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester;(16R)-E-Isositsirikine;NSC 282700;NSC 338932;Rhazimanine;Indolo[2,3-a]quinolizine-2-acetic acid, 3-ethylidene-1,2,3,4,6,7,12,12b-octahydro-α-(hydroxymethyl)-, methyl ester, (αR,2R,3E,12bS)-;17,18-Secoyohimban-16-carboxylicacid,19,20-didehydro-17-hydroxy-,methylester | | CAS: | 6519-27-3 | | MF: | C21H26N2O3 | | MW: | 354.45 | | EINECS: | | | Product Categories: | | | Mol File: | 6519-27-3.mol |  |
| | 16-epi-isositsirikine Chemical Properties |
| Melting point | 263.5℃ | | Boiling point | 558.9±50.0 °C(Predicted) | | density | 1.26±0.1 g/cm3(Predicted) | | pka | 14.29±0.10(Predicted) |
| | 16-epi-isositsirikine Usage And Synthesis |
| Description | An amorphous alkaloid found in Vinca rosea L., this laevorotatory base has
[α]25D - 20° (CHCI3). In EtOH, the ultraviolet spectrum has absorption maxima
at 224, 283 and 291 m/J.. The alkaloid forms a hemisulphate, m.p. 263.5°C and
an amorphous O-acetate. The picrate is obtained in the form of brilliant yellow
needles when crystallized from MeOH, m.p. 216°C. | | Uses | (16R)-E-Isositsirikine is an indole alkaloid compound from Catharanthus roseus Tissue Cultures IV1[1]. | | Definition | ChEBI: 16R,19E-isositsirikine is an alkaloid. It has a role as a metabolite. | | References | Kutney, Brown., Tetrahedron, 22,321 (1966) |
| | 16-epi-isositsirikine Preparation Products And Raw materials |
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