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20-ethyl-8-hydroxy-1,16-dimethoxy-4-(methoxymethyl)aconitan-14-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71239-55-9

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71239-55-9 Usage

Structure

Contains an aconitane core, an acetoxy substituent, and multiple methoxy groups

Aconitane

Toxic alkaloid found in plants

Acetate Group

Indicates derivative of acetic acid

Functional Groups

Hydroxy, methoxy, and ethyl groups present

Biological Activity

Potential for interaction with biological molecules

Toxicity

Due to complex and potentially toxic nature, handle with caution

Research/Industrial Use

Properties should be thoroughly investigated before application in research or industry.

Check Digit Verification of cas no

The CAS Registry Mumber 71239-55-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,2,3 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 71239-55:
(7*7)+(6*1)+(5*2)+(4*3)+(3*9)+(2*5)+(1*5)=119
119 % 10 = 9
So 71239-55-9 is a valid CAS Registry Number.

71239-55-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 14-acetyl-8-O-methyltalatizamine

1.2 Other means of identification

Product number -
Other names Aconitane-8,14-diol,20-ethyl-1,16-dimethoxy-4-(methoxymethyl)-,14-acetate,(1alpha,14alpha,16beta)

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:71239-55-9 SDS

71239-55-9Downstream Products

71239-55-9Relevant academic research and scientific papers

ALKALOIDS OF ACONITUM COLUMBIANUM NUTT.

Pelletier, S. William,Srivastava, Santosh K.,Joshi, Balawant S.

, p. 331 - 338 (2007/10/02)

The alkaloidal constituents of Aconitum columbianum Nutt. ssp. columbianum have been investigated.In addition to the known alkaloids cammaconine (12), deltaline (10), dictyocarpine (11), talatizamine (3), and 8-O-methyltalatizamine (7), a new base columbidine (4) has been isolated and its structure elucidated.The structure was derived on the basis of spectral data and chemical correlation with talatizamine.Synthesis of 7 from talatizamine is described and the 13C-nmr spectrum of 14-dehydrotalatizamine has been recorded.Certain 13C-nmr signals for these compounds have been reassigned.

ALKALOIDS OF ACONITUM COLUMBIANUM NUTT.

Boido, Vito,Edwards, Oliver E.,Handa, Kashmiri L.,Kolt, Ralph J.,Purushothaman, Koziparambil K.

, p. 778 - 784 (2007/10/02)

The most abundant readily isolated alkaloids of the aerial portion of Aconitum columbianum Nutt. were found to be talatisamine and cammaconine.New spectral data for known derivatives of these alkaloids and descriptions of new derivatives are presented.Less abundant alkaloids identified included the known ones sachaconitine, talatizidine, isotalatizidine, and 14-O-acetyltalatisamine, and the new ones 8-O-methyltalatisamine and a tetrahydroxymonomethoxy alkaloid, columbianine, with the same oxygenation pattern and stereochemistry as cammaconine.

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