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(16xi,17R,19E)-ajmal-19-en-17-ol is a specific stereoisomer of ajmaline, a naturally occurring alkaloid found in plants such as Rauwolfia serpentina and Catharanthus roseus. It has a complex molecular structure, characterized by a 19 carbon backbone with a hydroxyl group at the 17th carbon and a double bond at the 19th carbon in the E configuration. The specific stereochemistry of (16xi,17R,19E)-ajmal-19-en-17-ol may influence its biological activity and potential therapeutic applications.

509-38-6

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509-38-6 Usage

Uses

Used in Pharmaceutical Industry:
(16xi,17R,19E)-ajmal-19-en-17-ol is used as a pharmaceutical compound for its potential antiarrhythmic and anti-inflammatory effects. Its specific stereochemistry may contribute to its biological activity, making it a promising candidate for further research and development in the pharmaceutical field.
Further research is needed to fully understand the functions and potential uses of this chemical compound, as well as to explore its potential applications in other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 509-38-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 509-38:
(5*5)+(4*0)+(3*9)+(2*3)+(1*8)=66
66 % 10 = 6
So 509-38-6 is a valid CAS Registry Number.

509-38-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name TETRAPHYLLICINE

1.2 Other means of identification

Product number -
Other names -

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

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More Details:509-38-6 SDS

509-38-6Relevant academic research and scientific papers

Stereoselective Transformation of Ajmaline into Three Minor Gelsemium Alkaloids, Koumidine, (19Z)-Anhydrovobasinediol and N-Demethoxyrankinidine and their Absolute Configuration

Kitajima, Mariko,Takayama, Hiromitsu,Sakai, Shin-ichiro

, p. 1773 - 1779 (2007/10/02)

Ajmaline was converted into new Gelsemium alkaloids, 19Z-anhydrovobasinediol and N-demethoxyrankinidine, via koumidine along the biomimetic sequence, and the absolute configuration of these alkaloids was determined by these transformations.

Partial Synthesis and the Absolute Configuration of Two New Gelsemium Alkaloids, Koumidine and (19Z)-Taberpsychine

Takayama, Hiromitsu,Kitajima, Mariko,Wongseripipatana, Sumphan,Sakai, Shin-ichiro

, p. 1075 - 1076 (2007/10/02)

The stereoselective transformation of ajmaline (3) into a new Gelsemium alkaloid, (19Z)-taberpsychine (1), via koumidine (2) is described.

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