structure of Ethyl 2-methylsulfonyl-4-trifluoromethyl-1,3-thiazole-5-carboxylate

Ethyl 2-methylsulfonyl-4-trifluoromethyl-1,3-thiazole-5-carboxylate

CAS No.: 1000339-78-5
M. Wt: 303.28
M. Fa: C8H8F3NO4S2
InChI Key: NWECTZZKNWFTHO-UHFFFAOYSA-N
Appearance: Solid

Names and Identifiers of 1000339-78-5

CAS Number

1000339-78-5

MDL Number

MFCD09750912

IUPAC Name

ethyl 2-methylsulfonyl-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate

InChI

InChI=1S/C8H8F3NO4S2/c1-3-16-6(13)4-5(8(9,10)11)12-7(17-4)18(2,14)15/h3H2,1-2H3

InChIKey

NWECTZZKNWFTHO-UHFFFAOYSA-N

Canonical SMILES

CCOC(=O)C1=C(N=C(S1)S(=O)(=O)C)C(F)(F)F

UNSPSC Code

12352100

Physical and chemical properties of 1000339-78-5

Molecular Formula

C8H8F3NO4S2

Molecular Weight

303.28

Safety Information of 1000339-78-5

Pictograms

Signal Word

 Warning

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of 1000339-78-5

Ethyl 2-methylsulfonyl-4-trifluoromethyl-1,3-thiazole-5-carboxylate has several applications across various fields:

  • Pharmaceutical Development: It serves as a building block for synthesizing novel therapeutic agents targeting infectious diseases and cancers.
  • Material Science: The compound is investigated for its potential in developing advanced materials, including polymers and coatings with specific properties due to its unique chemical structure.
  • Agricultural Chemistry: Its antimicrobial properties make it a candidate for use in agricultural formulations aimed at pest control.

Interaction Studies of 1000339-78-5

Studies on Ethyl 2-methylsulfonyl-4-trifluoromethyl-1,3-thiazole-5-carboxylate reveal its interactions with various biological targets:

  • Enzyme Binding Studies: Research has shown that this compound can bind to specific enzymes, inhibiting their activity and thereby influencing biochemical pathways.
  • Receptor Interaction: The compound's structural features allow it to interact with certain receptors involved in disease processes, making it a candidate for drug development.

Biological Activity of 1000339-78-5

Research indicates that compounds similar to Ethyl 2-methylsulfonyl-4-trifluoromethyl-1,3-thiazole-5-carboxylate exhibit diverse biological activities, including:

  • Antimicrobial Properties: Thiazole derivatives are known for their potential in combating bacterial and fungal infections.
  • Anticancer Activity: Some studies suggest that such compounds may inhibit tumor growth and induce apoptosis in cancer cells.
  • Enzyme Inhibition: The compound may interact with specific enzymes or receptors, modulating their activity, which is crucial for therapeutic applications.