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3-{[2-(3,4-dimethoxyphenyl)ethyl]amino}cyclopent-2-en-1-one is a complex organic compound with a molecular formula of C18H23NO3. It features a cyclopent-2-en-1-one core structure, which is a five-membered ring with a double bond and a ketone group. Attached to this core is an amino group, which is connected to a 2-(3,4-dimethoxyphenyl)ethyl chain. The 3,4-dimethoxyphenyl group consists of a benzene ring with two methoxy substituents at the 3rd and 4th positions. 3-{[2-(3,4-dimethoxyphenyl)ethyl]amino}cyclopent-2-en-1-one is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting the dopamine D2 receptor, due to its structural similarity to certain psychoactive substances. It is important to note that while it shares structural elements with such compounds, its specific effects, safety, and legal status can vary, and it is not approved for medical use. The compound is typically synthesized in a laboratory setting and is subject to strict regulations regarding its production, distribution, and use.

53129-00-3

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53129-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53129-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,2 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53129-00:
(7*5)+(6*3)+(5*1)+(4*2)+(3*9)+(2*0)+(1*0)=93
93 % 10 = 3
So 53129-00-3 is a valid CAS Registry Number.

53129-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[2-(3,4-dimethoxyphenyl)ethylamino]cyclopent-2-en-1-one

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

1.4 Supplier's details

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More Details:53129-00-3 SDS

53129-00-3Downstream Products

53129-00-3Relevant academic research and scientific papers

ANODIC INTRAMOLECULAR ARYLATION OF ENAMINONES

Eilenberg, W.,Schaefer, H. J.

, p. 5023 - 5026 (2007/10/02)

N-Benzyl- and β-phenethyl-enaminones are cyclized at the anode to isoquinolines and benzazepines.

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