466-57-9

Basic information

• Product Name: (17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate
• Synonyms: (17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate;Rauvomitine;Rauvomitin
• CAS NO: 466-57-9
• Molecular Formula: C30H34N2O5
• Molecular Weight: 502.6
• Mol File: 466-57-9.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Density: 1.33g/cm³
• Refractive Index: 1.657
• CAS DataBase Reference: (17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: (17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate(466-57-9)
• EPA Substance Registry System: (17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate(466-57-9)

Safety Data

• Hazardous Substances Data: 466-57-9(Hazardous Substances Data)

Usage

Description

(17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate is an alkaloid derived from Rauwolfia vomitora, a plant source. It forms colorless crystals when dissolved in methanol (MeOH) and exhibits a specific optical rotation of [α]D 173.4° ± 1° (c 1.0, CHCl3). The hydrochloride salt of this compound has a melting point of 223°C (dec.). Upon acid hydrolysis, it yields tetraphyllicine and gallic acid trimethyl ether.

Uses

1. Used in Pharmaceutical Industry:
(17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate is used as a pharmaceutical compound for its potential therapeutic applications. The alkaloid's unique structure and properties make it a candidate for further research and development in the field of medicine.
2. Used in Chemical Research:
(17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate is also used as a subject of study in chemical research, particularly in the investigation of alkaloids, their properties, and potential applications in various fields.
3. Used in Plant Source Studies:
As an alkaloid derived from Rauwolfia vomitora, (17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate contributes to the understanding of the plant's chemical constituents and their potential uses in various industries, including pharmaceuticals and agriculture.

References

Haack, Popelak, Springler., Naturwiss., 42,627 (1955) Poisson, Goutarel, Janot., Compt. rend., 241, 1840 (1955) Bartlett et al., J. Amer. Chem. Soc., 84,622 (1962)

InChI:InChI=1/C30H34N2O5/c1-6-16-15-32-21-13-18(16)25-22(32)14-30(19-9-7-8-10-20(19)31(2)27(21)30)28(25)37-29(33)17-11-23(34-3)26(36-5)24(12-17)35-4/h6-12,18,21-22,25,27-28H,13-15H2,1-5H3/b16-6-/t18-,21-,22-,25+,27?,28?,30+/m0/s1