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2,4-dioxopyrrolidine-1-acetamide, also known as pyrrolidin-2,4-dione-1-acetamide, is a pyrrolidinone derivative that serves as a versatile building block in the synthesis of pharmaceuticals and organic compounds. This white crystalline solid, with a molecular formula of C5H7NO3 and a molecular weight of 129.11 g/mol, is recognized for its diverse applications in chemistry and pharmaceuticals due to its adaptable chemical properties.

85614-54-6

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85614-54-6 Usage

Uses

Used in Pharmaceutical Synthesis:
2,4-dioxopyrrolidine-1-acetamide is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure and reactivity make it a valuable component in medicinal chemistry.
Used in Organic Synthesis:
In the field of organic synthesis, 2,4-dioxopyrrolidine-1-acetamide is utilized as an intermediate, facilitating the creation of a wide range of organic compounds. Its ability to participate in various chemical reactions enhances its utility in organic chemistry.
Used in Agrochemical Production:
2,4-dioxopyrrolidine-1-acetamide is employed as an intermediate in the manufacturing of agrochemicals, playing a crucial role in the development of agricultural products such as pesticides and herbicides. Its involvement in these processes helps to improve crop protection and yield.
Used as a Reagent in Organic Synthesis:
2,4-dioxopyrrolidine-1-acetamide also serves as a reagent in organic synthesis, enabling chemists to perform specific reactions and transformations. Its versatility in this capacity supports the advancement of organic chemistry research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 85614-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,1 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85614-54:
(7*8)+(6*5)+(5*6)+(4*1)+(3*4)+(2*5)+(1*4)=146
146 % 10 = 6
So 85614-54-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2O3/c7-5(10)3-8-2-4(9)1-6(8)11/h1-3H2,(H2,7,10)

85614-54-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,4-dioxopyrrolidin-1-yl)acetamide

1.2 Other means of identification

Product number -
Other names 1-Pyrrolidineacetamide,2,4-dioxo

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:85614-54-6 SDS

85614-54-6Relevant academic research and scientific papers

A oxiracetam key intermediate 2 - (2, 4 - dioxo-pyrrolidine - 1 - yl) - acetamide synthesis process

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Paragraph 0020; 0021, (2017/08/25)

The invention provides a novel synthesis process for preparing an oxiracetam key intermediate 2-(2,4-dioxopyrrolidine-1-yl)-acetamide by using 4-halogenated acetoacetic ester and glycinamide hydrochloride as raw materials by virtue of a 'one-pot method'. The novel synthesis process has the advantages of being few in reaction steps, high in yield, cheap and easily available in raw materials, simple in post-treatment, has few waste gas, waste water and waste residues and the like.

A oxiracetam intermediate and its preparation method and application

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Paragraph 0152-0155, (2017/08/31)

The invention provides an oxiracetam intermediate as well as a preparation method and application thereof. The oxiracetam intermediate is a solid or a crystalline solid, low in preparation cost, and easy to purify and store, and can be used for efficiently preparing oxiracetam. The structural formula is as shown in the specifications.

New enantioselective synthesis of 4-hydroxy-2-oxopyrrolidine-N-acetamide (oxiracetam) from malic acid

Almeida,Anaya,Martin,Grande,Moran,Cruz Caballero

, p. 1431 - 1440 (2007/10/02)

The enantioselective synthesis of oxiracetam has been accomplished from readily available optically active D(+) and L(-) malic acids. the key step of the described method involves the selective reduction of a chiral cyclic diimide; in this way, both enantiomers of 4-hydroxy-2-oxopyrrolidine-N-acetamides were prepared.

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