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10,11-dimethoxy-5,6-dihydro[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinolin-7-ium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19716-72-4

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19716-72-4 Usage

Chemical class

Isoquinoline

Explanation

The compound belongs to the isoquinoline class of compounds, which are a group of naturally occurring and synthetic organic compounds with a bicyclic structure.

Explanation

The compound has a complex molecular structure, featuring a quaternary ammonium salt, two methoxy groups, and a dioxolo ring.

Explanation

The compound is a heterocyclic organic compound, meaning it contains a ring of atoms with at least one atom being different from carbon.

Explanation

The compound contains a quaternary ammonium salt, which is a positively charged ion with four organic groups attached to a central nitrogen atom.

Explanation

The compound has two methoxy groups, which are -OCH3 groups attached to the molecule.

Explanation

The compound features a dioxolo ring, which is a five-membered ring containing two oxygen atoms.

Explanation

Due to its unique molecular structure and potential biological activity, the compound may have applications in pharmaceutical research and drug development.

Explanation

The compound's precise properties and potential uses would require further analysis and research to fully understand its capabilities and limitations.

Explanation

The compound's unique molecular structure suggests that it may have potential biological activity, which could be explored for various applications.

Explanation

The solubility of the compound in different solvents is not provided in the material and would require further investigation.

Molecular structure

Complex

Heterocyclic organic compound

Yes

Quaternary ammonium salt

Yes

Methoxy groups

Two

Dioxolo ring

Present

Potential applications

Pharmaceutical research and drug development

Further analysis and research needed

Yes

Biological activity

Potential

Solubility

Unknown

Check Digit Verification of cas no

The CAS Registry Mumber 19716-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,1 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19716-72:
(7*1)+(6*9)+(5*7)+(4*1)+(3*6)+(2*7)+(1*2)=134
134 % 10 = 4
So 19716-72-4 is a valid CAS Registry Number.

19716-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 10,11-dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinolinylium

1.2 Other means of identification

Product number -
Other names 10,11-dimethoxy-5,6-dihydro[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinolin-7-ium

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:19716-72-4 SDS

19716-72-4Downstream Products

19716-72-4Relevant academic research and scientific papers

A General, Concise Strategy that Enables Collective Total Syntheses of over 50 Protoberberine and Five Aporhoeadane Alkaloids within Four to Eight Steps

Zhou, Shiqiang,Tong, Rongbiao

, p. 7084 - 7089 (2016/05/19)

A concise, catalytic, and general strategy that allowed efficient total syntheses of 22 natural 13-methylprotoberberines within four steps for each molecule is reported. This synthesis represents the most efficient and shortest route to date, featuring three catalytic processes: CuI-catalyzed redox-A3 reaction, Pd-catalyzed reductive carbocyclization, and PtO2-catalyzed hydrogenation. Importantly, this new strategy to the tetracyclic framework has also been applied to the collective concise syntheses of >30 natural protoberberines (without 13-methyl group) and five aporhoeadane alkaloids.

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