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(8alpha)-5'alpha-benzyl-12'-hydroxy-2'-isopropylergotaman-3',6',18-trione is a complex organic compound derived from the ergot fungus, which is known for its various alkaloids with diverse pharmacological properties. This specific compound is characterized by its unique molecular structure, featuring a benzyl group and hydroxyl functional groups, which may contribute to its potential applications in various fields.

511-07-9

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511-07-9 Usage

Uses

Used in Pharmaceutical Applications:
(8alpha)-5'alpha-benzyl-12'-hydroxy-2'-isopropylergotaman-3',6',18-trione is used as a pharmaceutical agent for its potential therapeutic effects. (8alpha)-5'alpha-benzyl-12'-hydroxy-2'-isopropylergotaman-3',6',18-trione's unique structure may allow it to interact with specific biological targets, such as receptors or enzymes, which could be beneficial in the treatment of certain medical conditions.
Used in Research and Development:
In the field of research and development, (8alpha)-5'alpha-benzyl-12'-hydroxy-2'-isopropylergotaman-3',6',18-trione can be used as a starting material or a reference compound for the synthesis of new ergot alkaloids or related compounds. Its structural features may provide insights into the design of novel molecules with improved pharmacological properties.
Used in Analytical Chemistry:
(8alpha)-5'alpha-benzyl-12'-hydroxy-2'-isopropylergotaman-3',6',18-trione can be employed as a reference compound in analytical chemistry for the development and validation of analytical methods, such as high-performance liquid chromatography (HPLC) or mass spectrometry (MS), for the detection and quantification of ergot alkaloids in various samples.
Used in Toxicology Studies:
As a mycotoxin found in moldy food products, (8alpha)-5'alpha-benzyl-12'-hydroxy-2'-isopropylergotaman-3',6',18-trione can be used in toxicology studies to investigate the effects of ergot alkaloids on human and animal health. This may help in understanding the mechanisms of toxicity and developing strategies for prevention and treatment of ergotism.
Used in Agriculture:
In the agricultural industry, (8alpha)-5'alpha-benzyl-12'-hydroxy-2'-isopropylergotaman-3',6',18-trione can be used as a marker compound for the detection and monitoring of ergot contamination in crops. This may help in ensuring food safety and quality by identifying and controlling the presence of toxic ergot alkaloids in the food supply.

Check Digit Verification of cas no

The CAS Registry Mumber 511-07-9 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 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 511-07:
(5*5)+(4*1)+(3*1)+(2*0)+(1*7)=39
39 % 10 = 9
So 511-07-9 is a valid CAS Registry Number.

511-07-9SDS

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 (5'α,8α)-5'-Benzyl-12'-hydroxy-2'-isopropyl-3',6',18-trioxoergota m

1.2 Other means of identification

Product number -
Other names Ergotaman-3‘,6‘,18-trione, 12‘-hydroxy-2‘-(1-methylethyl)-5‘-(phenylmethyl)-, (5‘-,8-)-

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:511-07-9 SDS

511-07-9Upstream product

511-07-9Downstream Products

511-07-9Relevant academic research and scientific papers

CONTRIBUTIONS TO THE STUDY OF EPIMERIZATION OF POLYPEPTIDIC ERGOT ALKALOIDS AT C-8

Bandula, Rodica,Vasilescu, Marilena

, p. 1189 - 1196 (2007/10/03)

The influence of pH and nature of the solvent upon the epimerization rate of polypeptidic ergot alkaloids (ergotamine, ergocristine, ergocryptine and ergocornine) at C-8 was studied.It was established that, in aqueous solutions, epimerization is minimum within 2.5-4.0 pH range.The first-order rate constants of epimerization in various organic solvents of the alkaloids in question were evaluated; they have shown that the epimerization rate is maximum in methanol, which is the most polar of the solvents tested.Epimerization at C-8 of ergotamine is a first-order reaction over a time interval much shorter than in epimerization of alkaloids from ergotoxine group, more so with methanol as solvent.Ether, chloroform and benzene have ensured an adequate stability.

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