2,5-dioxooxazolidine-4-propionic acid

  • Name: 2,5-dioxooxazolidine-4-propionic acid
  • CAS: 3981-39-3
  • Purity: 99%
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1.What is the 2,5-dioxooxazolidine-4-propionic acid ?

Used in Pharmaceutical and Agrochemical Industries:
2,5-dioxooxazolidine-4-propionic acid is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with enhanced properties and improved efficacy.
Used in Dye Production:
2,5-dioxooxazolidine-4-propionic acid is also utilized in the production of reactive dyes, which are widely used in the textile industry for their ability to form strong bonds with fibers, resulting in vibrant and long-lasting colors.
Used in Polymer Chemistry:
2,5-dioxooxazolidine-4-propionic acid has been studied for its potential use in polymer chemistry, specifically in the development of new materials with enhanced properties. Its incorporation into polymers can lead to improved mechanical strength, thermal stability, and other desirable characteristics.
However, due to the complex structure and potential reactivity of 2,5-dioxooxazolidine-4-propionic acid, it requires careful handling and storage to avoid any potential hazards. This ensures the safety of workers and the environment while maximizing the compound's potential in various applications.

L-N-benzyloxycarbonylglutamic acid

L-N-benzyloxycarbonylglutamic acid

3-(2,5-dioxo-oxazolidin-4-yl)-propionic acid
3981-39-3,33043-68-4

3-(2,5-dioxo-oxazolidin-4-yl)-propionic acid

Conditions
Conditions Yield
With benzoic acid; In butanone; at 80 ℃; for 29h; Inert atmosphere; Molecular sieve;
89%
L-glutamic acid
56-86-0,21675-62-7,23009-64-5,25104-13-6,84960-48-5,25513-46-6

L-glutamic acid

3-(2,5-dioxo-oxazolidin-4-yl)-propionic acid
3981-39-3,33043-68-4

3-(2,5-dioxo-oxazolidin-4-yl)-propionic acid

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1.1: tetra(n-butyl)ammonium hydroxide / butanone; methanol / 0.5 h / 20 °C / Inert atmosphere; Molecular sieve
1.2: 20 h / Inert atmosphere
2.1: benzoic acid / butanone / 29 h / 80 °C / Inert atmosphere; Molecular sieve
With tetra(n-butyl)ammonium hydroxide; benzoic acid; In methanol; butanone;

2.What is the CAS number for 2,5-dioxooxazolidine-4-propionic acid ?

The CAS number of 2,5-dioxooxazolidine-4-propionic acid is 3981-39-3.

More information of 2,5-dioxooxazolidine-4-propionic acid 3981-39-3 are:

CAS?Number

3981-39-3

Density

1.473g/cm3

Boiling Point

°Cat760mmHg

Flash Point

°C

Refractive Index

1.5

3.What are another words for 2,5-dioxooxazolidine-4-propionic acid ?

Synonyms?for?2,5-dioxooxazolidine-4-propionic acid 3981-39-3:

4.What is the molecular formula of 2,5-dioxooxazolidine-4-propionic acid?

The chemical formula of ?2,5-dioxooxazolidine-4-propionic acid is?C6 H7 NO5 which containing 6 Carbon atoms,7 Hydrogen atoms,1 Nitrogen atoms and 5 Oxygen atoms,and the molecular weight of??2,5-dioxooxazolidine-4-propionic acid?is 173.125.

5.What is 2,5-dioxooxazolidine-4-propionic acid (3981-39-3) used for?

2,5-dioxooxazolidine-4-propionic acid, also known as 2,5-dioxo-4-oxazolidinepropanoic acid, is a chemical compound with the molecular formula C5H5NO4. It is a white crystalline solid that is soluble in water and has a molecular weight of 147.09 g/mol. 2,5-dioxooxazolidine-4-propionic acid is primarily used as a synthetic intermediate in the production of various pharmaceuticals and agrochemicals, particularly in the synthesis of beta-lactam antibiotics and other biologically active molecules. Its chemical structure consists of a five-membered oxazolidine ring with a propionic acid side chain, featuring two carbonyl groups at the 2 and 5 positions. Due to its reactivity and versatility, 2,5-dioxooxazolidine-4-propionic acid plays a significant role in the development of new drugs and chemical compounds with potential therapeutic applications.

InChI:InChI=1/C6H7NO5/c8-4(9)2-1-3-5(10)12-6(11)7-3/h3H,1-2H2,(H,7,11)(H,8,9)

Relevant articles related to 2,5-dioxooxazolidine-4-propionic acid:

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Source

PREPARATION OF ORGANIC COMPOUNDS FOR ENHANCED REACTIVITY

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Page/Page column 9, (2010/06/16)

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