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2,5-dioxo-1-Pyrrolidinepropanal, also known as 2,5-dioxopiperazine-3-propanal or 2,5-dioxo-3-piperidinonepropanal, is an organic compound with the chemical formula C6H7NO3. It is a cyclic imine derivative of piperidine, featuring a pyrrolidine ring with a propanal group attached to the 1-position and two oxygen atoms at the 2 and 5 positions, forming a dioxo group. 2,5-dioxo-1-Pyrrolidinepropanal is a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those containing the piperidine ring system. It is also used in the preparation of 1,4-dihydropyridines, which are important in the treatment of cardiovascular diseases. The compound is typically synthesized through the reaction of 1,4-dicarbonyl compounds with primary amines, followed by oxidation. Due to its reactivity and potential applications, 2,5-dioxo-1-Pyrrolidinepropanal is of significant interest in the field of organic chemistry and drug development.

5615-85-0

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5615-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5615-85-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,1 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5615-85:
(6*5)+(5*6)+(4*1)+(3*5)+(2*8)+(1*5)=100
100 % 10 = 0
So 5615-85-0 is a valid CAS Registry Number.

5615-85-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,5-dioxo-pyrrolidin-1-yl)propionaldehyde

1.2 Other means of identification

Product number -
Other names N-(3-Oxo-propyl)-succinimid

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

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More Details:5615-85-0 SDS

5615-85-0Relevant academic research and scientific papers

Self-assembled bidentate ligands for ru-catalyzed anti-Markovnikov hydration of terminal alkynes

Chevallier, Floris,Breit, Bernhard

, p. 1599 - 1602 (2006)

(Figure Presented) In pairs: Bidentate ligands are generated by the self-assembly of monodentate ligands through complementary hydrogen bonding. A ruthenium complex bearing such self-assembled heterodimeric ligands is used as the catalyst in the regioselective hydration of terminal alkynes. FG = functional group, Piv = pivaloyl.

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