4-Oxazolidineaceticacid, 2,5-dioxo-

  • Name: 4-Oxazolidineaceticacid, 2,5-dioxo-
  • CAS: 6542-24-1
  • Purity: 99%
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Quality products?make an important contribution to long-term revenue and profitability. Top quality factory supply 6542-24-1 4-Oxazolidineaceticacid, 2,5-dioxo- at low price

1.What is the 4-Oxazolidineaceticacid, 2,5-dioxo- ?

phosgene
75-44-5

phosgene

L-Aspartic acid
56-84-8,25608-40-6,27881-03-4,32505-46-7,52526-39-3

L-Aspartic acid

L-2,5-Dioxo-4-oxazolidinessigsaeure
33043-53-7,6542-24-1

L-2,5-Dioxo-4-oxazolidinessigsaeure

Conditions
Conditions Yield
In tetrahydrofuran; Ambient temperature;

2.What is the CAS number for 4-Oxazolidineaceticacid, 2,5-dioxo- ?

The CAS number of 4-Oxazolidineaceticacid, 2,5-dioxo- is 6542-24-1.

More information of 4-Oxazolidineaceticacid, 2,5-dioxo- 6542-24-1 are:

CAS?Number

6542-24-1

Density

1.575g/cm3

Refractive Index

1.504

PSA

96.19000

LogP

-1.26390

3.What are another words for 4-Oxazolidineaceticacid, 2,5-dioxo- ?

Synonyms?for?4-Oxazolidineaceticacid, 2,5-dioxo- 6542-24-1:2,5-dioxooxazolidine-4-acetic acid

4.What is the molecular formula of 4-Oxazolidineaceticacid, 2,5-dioxo-?

The chemical formula of ?4-Oxazolidineaceticacid, 2,5-dioxo- is?C5 H5 NO5 which containing 5 Carbon atoms,5 Hydrogen atoms,1 Nitrogen atoms and 5 Oxygen atoms,and the molecular weight of??4-Oxazolidineaceticacid, 2,5-dioxo-?is 159.098.

5.What is 4-Oxazolidineaceticacid, 2,5-dioxo- (6542-24-1) used for?

4-Oxazolidineacetic acid, 2,5-dioxo-, also known as 2,5-Dioxo-4-oxazolidineacetic acid or 4-Oxazolidine-2,5-dione, is a heterocyclic organic compound with the chemical formula C3H5NO3. It features a five-membered oxazolidine ring with a carbonyl group at the 2-position and a carboxyl group at the 5-position. 4-Oxazolidineaceticacid, 2,5-dioxo- is a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those containing the 4-oxazolidinone moiety. It is also used in the production of beta-lactam antibiotics, such as penicillins and cephalosporins, due to its ability to form stable rings and contribute to the overall stability of the drug molecules. The compound is typically synthesized through various chemical reactions, such as the condensation of amino acids with aldehydes or ketones, and is known for its reactivity and potential applications in the development of new drugs and chemical compounds.

InChI:InChI=1/C5H5NO5/c7-3(8)1-2-4(9)11-5(10)6-2/h2H,1H2,(H,6,10)(H,7,8)

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