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55529-55-0

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55529-55-0 Usage

Description

17β-Hydroxy-19α-methyl-18-oxayohimban-16α-carboxylic acid methyl ester is a complex organic compound with a unique molecular structure. It is an alkaloid derived from the root bark of Cabucala striolata and has been characterized through chemical and spectroscopic methods. 17β-Hydroxy-19α-methyl-18-oxayohimban-16α-carboxylic acid methyl ester features a hydroxyl group at the 17β position, a methyl group at the 19α position, an oxo group at the 18 position, and a carboxylic acid methyl ester at the 16α position. Its intricate structure suggests potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
17β-Hydroxy-19α-methyl-18-oxayohimban-16α-carboxylic acid methyl ester is used as a pharmaceutical compound for its potential therapeutic properties. 17β-Hydroxy-19α-methyl-18-oxayohimban-16α-carboxylic acid methyl ester's unique structure may allow it to interact with specific biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, 17β-Hydroxy-19α-methyl-18-oxayohimban-16α-carboxylic acid methyl ester serves as a valuable subject for studying the synthesis, reactivity, and potential applications of complex organic molecules. Its unique structure can provide insights into the development of new synthetic methods and the exploration of novel chemical reactions.
Used in Drug Delivery Systems:
Similar to gallotannin, 17β-Hydroxy-19α-methyl-18-oxayohimban-16α-carboxylic acid methyl ester could be employed in drug delivery systems to enhance its bioavailability and therapeutic outcomes. By incorporating the compound into various carriers, such as organic or metallic nanoparticles, its delivery and efficacy against specific targets can be improved.

References

Bombardelli et al., Fitoterapia, 45, 183 (1974)

Check Digit Verification of cas no

The CAS Registry Mumber 55529-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,2 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55529-55:
(7*5)+(6*5)+(5*5)+(4*2)+(3*9)+(2*5)+(1*5)=140
140 % 10 = 0
So 55529-55-0 is a valid CAS Registry Number.

55529-55-0SDS

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 ajmalicinine

1.2 Other means of identification

Product number -
Other names (7aR,8S,10R,11R,11aS,12aS)-10-Hydroxy-8-methyl-5,6,7a,8,10,11,11a,12,12a,13-decahydro-7H-9-oxa-6a,13-diaza-indeno[2,1-a]anthracene-11-carboxylic acid methyl ester

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:55529-55-0 SDS

55529-55-0Relevant articles and documents

HETEROYOHIMBINE ALKALOID SYNTHESIS

Jokela, Reija,Taipale, Tuula,Ala-Kaila, Kari,Lounasmaa, Mauri

, p. 2265 - 2271 (2007/10/02)

Preparation of the heteroyohimbine analogues 6 and 7 and a new short stereoselective total synthesis of (+/-)-3-iso-19-epiajmalicine 12 are described.

Heteroyohimbine Alkaloids. Stereospecific Conversion of Ajmalicine into 19-Epiajmalicine

Palmisano, Giovanni,Danieli, Bruno,Lesma, Giordano,Riva, Renata

, p. 923 - 926 (2007/10/02)

An efficient four-step sequence to 19-epiajmalicine, a rare heteroyohimbane alkaloid, which requires mild conditions and utilises ajmalicine as an easily accessible starting material, is described.

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