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3-[3-(dimethylamino)propanoyl]-2H-chromen-2-one is a complex organic compound with the molecular formula C15H16NO4. It is a derivative of the naturally occurring flavonoid, flavone, which is characterized by a benzopyrone structure. This specific compound features a dimethylamino group attached to a propanoyl chain that is further linked to the flavone core. It is known for its potential biological activities, such as antioxidant and anti-inflammatory properties, and is found in various plants. The compound's structure and properties make it a subject of interest in pharmaceutical and chemical research, particularly for its potential applications in the development of new drugs and therapeutic agents.

5461-41-6

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5461-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5461-41-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5461-41:
(6*5)+(5*4)+(4*6)+(3*1)+(2*4)+(1*1)=86
86 % 10 = 6
So 5461-41-6 is a valid CAS Registry Number.

5461-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[3-(dimethylamino)propanoyl]chromen-2-one,hydrochloride

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

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More Details:5461-41-6 SDS

5461-41-6Downstream Products

5461-41-6Relevant academic research and scientific papers

Synthesis of 3-(6-aryl-pyridin-2-yl)- and 8-(6-aryl-pyridin-2-yl) coumarins

Brahmbhatt,Gajera,Pandya,Patel

, p. 869 - 871 (2008/09/18)

Mannich bases of 3-acetyl coumarin 1 and 4-methyl-7-methoxy-8-acetyl coumarin 4 on reaction with substituted phenacyl bromide pyridinium salts 2a-f in the presence of ammonium acetate in refluxing acetic acid afford the title 3-(6-aryl-pyridin-2-yl)- and 8-(6-aryl-pyridin-2-yl) coumarins (3a-f and 5a-f) in moderate to good yields.

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