structure of 3-(4-Chlorothiophen-2-yl)propanoic acid

3-(4-Chlorothiophen-2-yl)propanoic acid

CAS No.: 89793-51-1
M. Wt: 190.65
M. Fa: C7H7ClO2S
InChI Key: AGGRDDNHSGUWGK-UHFFFAOYSA-N

Names and Identifiers of 3-(4-Chlorothiophen-2-yl)propanoic acid

CAS Number

89793-51-1

MDL Number

MFCD18324747

IUPAC Name

3-(4-chlorothiophen-2-yl)propanoic acid

InChI

InChI=1S/C7H7ClO2S/c8-5-3-6(11-4-5)1-2-7(9)10/h3-4H,1-2H2,(H,9,10)

InChIKey

AGGRDDNHSGUWGK-UHFFFAOYSA-N

Canonical SMILES

C1=C(SC=C1Cl)CCC(=O)O

UNSPSC Code

12352100

Physical and chemical properties of 3-(4-Chlorothiophen-2-yl)propanoic acid

H Bond Acceptors

2

H Bond Donors

1

LogP

2.57248881966667

Molecular Formula

C7H7ClO2S

Molecular Weight

190.65

Safety Information of 3-(4-Chlorothiophen-2-yl)propanoic acid

Pictograms

Signal Word

 Warning

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

Applications of 3-(4-Chlorothiophen-2-yl)propanoic acid

3-(4-Chlorothiophen-2-yl)propanoic acid has diverse applications:

  • Organic Synthesis: It serves as a building block for synthesizing more complex organic molecules.
  • Biological Research: Used in studies related to enzyme inhibition and protein interactions.
  • Material Science: Potential applications in developing new materials with specific electronic or optical properties.

Interaction Studies of 3-(4-Chlorothiophen-2-yl)propanoic acid

Research indicates that 3-(4-Chlorothiophen-2-yl)propanoic acid interacts with various biological targets, which may include enzymes and receptors involved in metabolic pathways. These interactions can lead to inhibition or modulation of specific biological processes, making it valuable in pharmacological studies. Further investigation into its binding affinities and mechanisms is essential for understanding its full potential.

Biological Activity of 3-(4-Chlorothiophen-2-yl)propanoic acid

3-(4-Chlorothiophen-2-yl)propanoic acid exhibits notable biological activity. It has been investigated for its potential role in enzyme inhibition and as a probe for biological assays. The specific mechanism of action often involves interaction with enzymes or receptors, leading to modulation of biochemical pathways. Its unique structure may contribute to its effectiveness in these roles.