4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione

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4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione

  • Name 4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione
  • CAS 23640-03-1
  • Purity 99%
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1.What is the 4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione ?

Used in Pharmaceutical Applications:
4-(1H-Imidazol-4-ylmethyl)oxazolidine-2,5-dione is used as an antimicrobial, antifungal, and antiviral agent for its ability to inhibit the growth of various microorganisms, which is attributed to its interaction with enzymes involved in the synthesis of DNA and RNA.
Used in Enzyme Inhibition:
In the field of biochemistry, 4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione is used as an enzyme inhibitor, targeting enzymes that play a role in nucleic acid synthesis, thereby affecting the replication and transcription processes in pathogens.
Used in Polymer Production:
4-(1H-Imidazol-4-ylmethyl)oxazolidine-2,5-dione is used as a monomer in the production of polymers, where its unique structure contributes to the formation of polymers with specific properties, such as enhanced stability or biocompatibility.
Used in Polymeric Material Synthesis:
As a crosslinking agent, 4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione is utilized in the synthesis of polymeric materials to improve their structural integrity and performance characteristics, such as mechanical strength and resistance to degradation.
Used in Biomedical Applications:
Due to its low toxicity and good biocompatibility, 4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione is used in the development of biomedical materials and devices, such as drug delivery systems, tissue engineering scaffolds, and medical coatings.
Used in Industrial Applications:
In various industries, 4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione is used for its potential as a component in the formulation of industrial products, such as coatings, adhesives, and composite materials, where its properties can enhance the performance and durability of these products.

N-[(benzyloxy)carbonyl]-L-histidine
14997-58-1

N-[(benzyloxy)carbonyl]-L-histidine

(<i>S</i>)-4-(1<sup>(3)</sup><i>H</i>-imidazol-4-ylmethyl)-oxazolidine-2,5-dione
23640-03-1

(S )-4-(1(3) H -imidazol-4-ylmethyl)-oxazolidine-2,5-dione

Conditions
Conditions Yield
With phosphorus tribromide; In tetrahydrofuran; at 25 ℃; for 2h;

2.What is the CAS number for 4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione ?

The CAS number of 4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione is 23640-03-1.

More information of 4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione 23640-03-1 are:

CAS?Number

23640-03-1

Density

1.526g/cm3

Boiling Point

°Cat760mmHg

Flash Point

°C

Refractive Index

1.602

HS CODE

2934999090

PSA

87.57000

LogP

-0.77280

3.What are another words for 4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione ?

Synonyms?for?4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione 23640-03-1:2,5-Oxazolidinedione,4-(1H-imidazol-4-ylmethyl)- (9CI); 2,5-Oxazolidinedione,4-(imidazol-4-ylmethyl)- (8CI); Histidine, N-carboxy-, cyclic anhydride

4.What is the molecular formula of 4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione?

The chemical formula of ?4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione is?C7H7 N3 O3 which containing 7 Carbon atoms,7 Hydrogen atoms,3 Nitrogen atoms and 3 Oxygen atoms,and the molecular weight of??4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione?is 181.151.

5.What is 4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione (23640-03-1) used for?

4-(1H-Imidazol-4-ylmethyl)oxazolidine-2,5-dione, also known as imidazolidine-2,5-dione, is a heterocyclic organic compound characterized by its cyclic urea derivative structure with a five-membered ring. It features both imidazole and oxazolidine moieties, which contribute to its potential pharmaceutical and industrial applications. 4-(1H-imidazol-4-ylmethyl)oxazolidine-2,5-dione has been recognized for its antimicrobial, antifungal, and antiviral properties, as well as its capacity to inhibit enzymes involved in DNA and RNA synthesis. Additionally, it has been considered for use as a monomer in polymer production and as a crosslinking agent in the synthesis of polymeric materials. Its low toxicity and good biocompatibility make it a promising candidate for a variety of biomedical and industrial uses.

InChI:InChI=1/C7H7N3O3/c11-6-5(10-7(12)13-6)1-4-2-8-3-9-4/h2-3,5H,1H2,(H,8,9)(H,10,12)

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