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1-[2-(3,4-dihydronaphthalen-1-yl)ethyl]pyrrolidine-2,5-dione is a pyrrolidine derivative that features a dihydronaphthalene group. This cyclic organic compound is characterized by a pyrrolidine-2,5-dione core structure with a dihydronaphthalene side chain attached to the nitrogen atom. Its unique molecular structure suggests potential applications in various fields, particularly in the pharmaceutical industry.
Used in Pharmaceutical Industry:
1-[2-(3,4-dihydronaphthalen-1-yl)ethyl]pyrrolidine-2,5-dione is used as a building block for drug synthesis due to its pyrrolidine derivative nature, which is known for its diverse biological activities. 1-[2-(3,4-dihydronaphthalen-1-yl)ethyl]pyrrolidine-2,5-dione may contribute to the development of new pharmaceuticals with specific therapeutic effects, pending further research to understand its properties and potential uses comprehensively.

4725-36-4

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4725-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4725-36-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,2 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4725-36:
(6*4)+(5*7)+(4*2)+(3*5)+(2*3)+(1*6)=94
94 % 10 = 4
So 4725-36-4 is a valid CAS Registry Number.

4725-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-(3,4-dihydronaphthalen-1-yl)ethyl]pyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names N-(2-<3,4-Dihydro-naphthyl-(1)>-ethyl)-bernsteinsaeureimid

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 -
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More Details:4725-36-4 SDS

4725-36-4Relevant academic research and scientific papers

Alkylation of Pyrrolidine-2,5-dione with 2-(3,4-Dihydro-1-napthalenyl)ethyl-4-methylphenylsulphonates: A New and General Approach to 13-Azaequilenin Analogs

Parihar,Ramana

, p. 11 - 18 (2007/10/03)

Pyrrolidine-2,5-dione was N-alkylated with three different 2-(3,4-dihydro-1-napthalenyl)ethyl-4-methylphenylsulphonates to give the corresponding seco-azasteroids which on chemoselective dehydrogenation, reduction with NaBH4 in MeOH at 0°C gave the corresponding 5-hydroxy-2-pyrrolidones. Intramolecular cyclization of these 5-hydroxy-2-pyrrolidones afforded the corresponding title compounds.

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