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(6alpha,14alpha,16beta)-13-hydroxy-1,6,16-trimethoxy-4-(methoxymethyl)-20-methylaconit-8(15)-en-14-yl benzoate is a complex chemical compound characterized by its molecular structure that contains multiple hydroxy, methoxy, and methyl groups. It features an aconitine moiety, a toxic alkaloid derived from plants of the Aconitum genus, which is esterified with benzoic acid to form a benzoate derivative. (6alpha,14alpha,16beta)-13-hydroxy-1,6,16-trimethoxy-4-(methoxymethyl)-20-methylaconit-8(15)-en-14-yl benzoate's structure, including the aconitine core and various functional groups, suggests potential pharmaceutical applications, although its toxic nature must be carefully considered.

60050-12-6

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60050-12-6 Usage

Uses

Used in Pharmaceutical Applications:
(6alpha,14alpha,16beta)-13-hydroxy-1,6,16-trimethoxy-4-(methoxymethyl)-20-methylaconit-8(15)-en-14-yl benzoate is used as a pharmaceutical compound for its potential neurotoxic and cardiotoxic effects. (6alpha,14alpha,16beta)-13-hydroxy-1,6,16-trimethoxy-4-(methoxymethyl)-20-methylaconit-8(15)-en-14-yl benzoate's structure, including the aconitine core, suggests that it may have applications in the development of drugs targeting the nervous and cardiovascular systems. However, its toxic nature requires careful consideration and further research to ensure safe and effective use.
Used in Research and Development:
In the field of scientific research, (6alpha,14alpha,16beta)-13-hydroxy-1,6,16-trimethoxy-4-(methoxymethyl)-20-methylaconit-8(15)-en-14-yl benzoate serves as a valuable compound for studying the effects of aconitine and its derivatives on biological systems. Its complex structure and functional groups make it an interesting subject for exploring potential interactions with receptors, enzymes, and other biological targets, which could lead to the discovery of new therapeutic agents or a better understanding of the mechanisms of action of related compounds.
Used in Traditional Medicine:
Historically, aconitine and its derivatives have been used in traditional medicine for their potent effects on the body. (6alpha,14alpha,16beta)-13-hydroxy-1,6,16-trimethoxy-4-(methoxymethyl)-20-methylaconit-8(15)-en-14-yl benzoate may be used in traditional medicine applications, where its neurotoxic and cardiotoxic properties are harnessed for specific therapeutic purposes. However, due to the compound's toxicity, its use in this context must be strictly regulated and guided by experienced practitioners to prevent adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 60050-12-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,5 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60050-12:
(7*6)+(6*0)+(5*0)+(4*5)+(3*0)+(2*1)+(1*2)=66
66 % 10 = 6
So 60050-12-6 is a valid CAS Registry Number.

60050-12-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Pyrodelphonine 14-benzoate

1.2 Other means of identification

Product number -
Other names pyrodelphinine

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:60050-12-6 SDS

60050-12-6Upstream product

60050-12-6Relevant academic research and scientific papers

The Pyrodelphonine Chromophore. Crystal Structures of Pyrodelphinine and Delphinine

Pelletier, S. William,Finer-Moore, Janet,Desai, Ranjit C.,Mody, Naresh V.,Desai, Haridutt K.

, p. 5290 - 5297 (2007/10/02)

The X-ray crystallographic analysis of pyrodelphinine (5) and delphinine (7) has established that the resonance structure 6 does not contribute to the structure of pyrodelphinine (5) in the electronic ground state.This result suggests that the free electr

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