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Eburnamenine is a naturally occurring alkaloid found in the plant family Rubiaceae, particularly in the plant species Gardenia jasminoides. It is known for its potential medicinal properties, including anti-inflammatory, analgesic, and antipyretic effects. Eburnamenine has been studied for its ability to inhibit the release of certain neurotransmitters, which may contribute to its pain-relieving and fever-reducing capabilities. However, it is important to note that while eburnamine has shown promise in laboratory settings, further research is needed to fully understand its safety and efficacy in clinical applications.

517-30-6

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517-30-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 517-30-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 517-30:
(5*5)+(4*1)+(3*7)+(2*3)+(1*0)=56
56 % 10 = 6
So 517-30-6 is a valid CAS Registry Number.

517-30-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (+) eburnamenine

1.2 Other means of identification

Product number -
Other names (11aR,11bR)-11a-Ethyl-2,3,4,5,11a,11b-hexahydro-1H-3a,9b-diaza-benzo[cd]fluoranthene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:517-30-6 SDS

517-30-6Relevant academic research and scientific papers

Synthetic Approach to (+/-)- Vincamine via Cleavage of an α-Diketone Monothioacetal. Alternative Synthesis of (+/-)-Eburnamine, (+/-)-Isoeburnamine, and (+/-)-Eburnamenine

Takano, Seiichi,Hatakeyama, Susumi,Ogasawara, Kunio

, p. 457 - 461 (2007/10/02)

The half ester (8) prepared from cleavage of 2-(1,3-dithian-2-yl)-4-ethoxycarbonyl-4-ethylcyclohexanone (7) has been converted into (+/-)-eburnamine (20), (+/-)-isoeburnamine (21), and (+/-)-eburnamenine (22) by a stereospecific reaction sequence proceeding via the dithian intermediate (16).However an attempted conversion of (16) into (+/-)-vincamine (6) was unsuccessful.

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