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1-[1-(3,4-dimethoxyphenyl)ethenyl]-6,7-dimethoxyisoquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58024-45-6

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58024-45-6 Usage

Chemical class

Isoquinoline alkaloids

Structure

Isoquinoline core
Two methoxy groups at positions 6 and 7
Phenyl group attached to the nitrogen atom at position 1 through a ethenyl linker

Occurrence

Commonly found in certain plants and organisms

Pharmacological activities

Anti-inflammatory
Antimicrobial
Anticancer

Research interest

Due to its unique structure and biological activities

Potential applications

Further research and potential therapeutic applications
This list provides a summary of the key properties and information about 1-[1-(3,4-dimethoxyphenyl)ethenyl]-6,7-dimethoxyisoquinoline, as described in the material provided.

Check Digit Verification of cas no

The CAS Registry Mumber 58024-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,2 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58024-45:
(7*5)+(6*8)+(5*0)+(4*2)+(3*4)+(2*4)+(1*5)=116
116 % 10 = 6
So 58024-45-6 is a valid CAS Registry Number.

58024-45-6SDS

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 1-[1-(3,4-dimethoxyphenyl)ethenyl]-6,7-dimethoxyisoquinoline

1.2 Other means of identification

Product number -
Other names 1-[1-(3,4-dimethoxyphenyl)vinyl]-6,7-dimethoxyisoquinoline

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:58024-45-6 SDS

58024-45-6Downstream Products

58024-45-6Relevant academic research and scientific papers

Iron-Catalyzed Aerobic Oxidation of (Alkyl)(aryl)azinylmethanes

Sterckx, Hans,Sambiagio, Carlo,Lemière, Filip,Tehrani, Kourosch Abbaspour,Maes, Bert U. W.

, p. 1564 - 1570 (2017/08/11)

An iron-catalyzed aerobic oxidation of (alkyl)(aryl)azinylmethanes has been developed leading to tertiary alcohols in moderate to good yields. Hock rearrangement was identified as a major side reaction leading to a complex mixture of undesired products. Addition of thiourea sometimes allows inhibiting this side reaction and steers the reaction towards the desired products.

SYNTHESIS OF 2,3,8,9-TETRAMETHOXY-11-PHENYL-5,6-DIHYDRODIBENZINDOLIZINE

Alarcon, Jorge A. R.,Soldatenkov, A. T.,Soldatova, S. A.,Samalloa, Alicia U.,Obando, Juan U.,Prostakov, N. S.

, p. 1054 - 1058 (2007/10/02)

2,3,8,9-Tetramethoxy-11-phenyldibenzindolizine was obtained in high yield from (6,7-dimethoxyisoquinolin-1-yl)-(3,4-dimethylphenyl)phenylcarbinol by cyclization in the presence of formic acid.The behavior of (6,7-dimethoxyisoquinolin-1-yl)-(3,4-dimethoxyphenyl)methylcarbinol and (6,7-dimethoxyisoquinolin-1-yl-(3,4-dimethoxyphenyl)carbinol was studied under these same conditions. 2,3,7,8-Tetramethoxy-11-phenyl-5,6-dihydrodibenzindolizine was obtained by hydrogenation on rhenium heptasulfide.

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