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24032-31-3

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24032-31-3 Usage

Chemical class

Isoquinoline alkaloids

Derivation

Reaction between 1-(3,4-dimethoxyphenyl)-2-nitroethenes and 1,2,3,4-tetrahydro-3-isoquinolone

Structural feature

1-(3,4-dimethoxybenzyl) group attached to the 6 and 7 positions of a dimethoxy-3-methylisoquinoline core

Pharmacological properties

Potential anti-inflammatory and antioxidant effects

Research interest

Structural complexity and unique chemical properties make it an interesting target for further research and potential drug development
These properties highlight the compound's classification, method of synthesis, structural characteristics, and areas of potential application in the field of pharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 24032-31-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,3 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24032-31:
(7*2)+(6*4)+(5*0)+(4*3)+(3*2)+(2*3)+(1*1)=63
63 % 10 = 3
So 24032-31-3 is a valid CAS Registry Number.

24032-31-3SDS

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-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-3-methylisoquinoline,hydrochloride

1.2 Other means of identification

Product number -
Other names 6,7-Dimethoxy-3-methyl-1-veratryl-isochinolin,Hydrochlorid

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:24032-31-3 SDS

24032-31-3Upstream product

24032-31-3Downstream Products

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