39965-06-5

Basic information

• Product Name: Victoxinine
• Synonyms: Victoxinine
• CAS NO: 39965-06-5
• Molecular Formula: C17H29NO
• Molecular Weight: 263.4183
• Mol File: 39965-06-5.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 361.9°Cat760mmHg
• Flash Point: 151.7°C
• Appearance: /
• Density: 1.03g/cm³
• Vapor Pressure: 1.07E-06mmHg at 25°C
• Refractive Index: 1.536
• PKA: 14.98±0.10(Predicted)
• CAS DataBase Reference: Victoxinine(CAS DataBase Reference)
• NIST Chemistry Reference: Victoxinine(39965-06-5)
• EPA Substance Registry System: Victoxinine(39965-06-5)

Safety Data

• Hazardous Substances Data: 39965-06-5(Hazardous Substances Data)

Usage

Description

Victoxinine is a steroidal alkaloid derived from Fritillaria verticillata var. Thunbergii, which is the ketone form of Verticine. Its structure has been confirmed through X-ray analysis of the methobromide, with a melting point of 287°C, using the heavy atom method.

Uses

1. Used in Pharmaceutical Industry:
Victoxinine is used as a pharmaceutical compound for its potential therapeutic applications. The expression is: Victoxinine is used as a pharmaceutical compound for its potential therapeutic applications due to its unique steroidal alkaloid structure and properties.
2. Used in Research and Development:
Victoxinine is used as a research compound for studying its chemical properties, structural analysis, and potential interactions with other molecules. The expression is: Victoxinine is used as a research compound for studying its chemical properties, structural analysis, and potential interactions with other molecules, which can contribute to the development of new drugs and therapies.
3. Used in Traditional Medicine:
Victoxinine may be used in traditional medicine for its potential medicinal properties, although further research is needed to validate its efficacy and safety. The expression is: Victoxinine is used in traditional medicine for its potential medicinal properties, but further research is required to confirm its efficacy and safety.

References

Pringle, Brown., Nature, 181,1205 (1958) Pringle, Brown., Phytopathology, SO, 324 (1960) Dorn, Arigoni., 1. Chern. Soc., Chern. Cornrnun., 1342 (19n)

InChI:InChI=1/C17H29NO/c1-11(2)13-5-6-17(4)12(3)14-9-18(7-8-19)10-15(17)16(13)14/h11,13-16,19H,3,5-10H2,1-2,4H3/t13-,14+,15+,16-,17+/m0/s1