structure of 1-(3-Chloro-4-fluorophenyl)pyrrolidine

1-(3-Chloro-4-fluorophenyl)pyrrolidine

CAS No.: 1000339-33-2
M. Wt: 199.65200
M. Fa: C10H11ClFN
InChI Key: RYEWSNZSVSTBSF-UHFFFAOYSA-N

Names and Identifiers of 1-(3-Chloro-4-fluorophenyl)pyrrolidine

CAS Number

1000339-33-2

MDL Number

MFCD09878399

IUPAC Name

1-(3-chloro-4-fluorophenyl)pyrrolidine

InChI

InChI=1S/C10H11ClFN/c11-9-7-8(3-4-10(9)12)13-5-1-2-6-13/h3-4,7H,1-2,5-6H2

InChIKey

RYEWSNZSVSTBSF-UHFFFAOYSA-N

Canonical SMILES

C1CCN(C1)C2=CC(=C(C=C2)F)Cl

UNSPSC Code

12352100

Physical and chemical properties of 1-(3-Chloro-4-fluorophenyl)pyrrolidine

Exact Mass

199.05600

H Bond Acceptors

1

H Bond Donors

0

LogP

3.14430

Molecular Formula

C10H11ClFN

Molecular Weight

199.65200

PSA

3.24000

Storage condition

2-8°C

Safety Information of 1-(3-Chloro-4-fluorophenyl)pyrrolidine

Pictograms

Signal Word

 Warning

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

Applications of 1-(3-Chloro-4-fluorophenyl)pyrrolidine

1-(3-Chloro-4-fluorophenyl)pyrrolidine has diverse applications across multiple domains:

  • Medicinal Chemistry: It is explored as a potential drug candidate due to its biological activity.
  • Organic Synthesis: The compound serves as a building block for synthesizing more complex molecules.
  • Industrial Use: It is utilized in producing specialty chemicals and intermediates for various applications.

Interaction Studies of 1-(3-Chloro-4-fluorophenyl)pyrrolidine

Studies focusing on the interactions of 1-(3-Chloro-4-fluorophenyl)pyrrolidine with biological targets have revealed insights into its mechanism of action. The compound may inhibit or activate specific enzymes or receptors, leading to various biochemical effects. Understanding these interactions is crucial for evaluating its therapeutic potential and safety profile.

Biological Activity of 1-(3-Chloro-4-fluorophenyl)pyrrolidine

Research indicates that 1-(3-Chloro-4-fluorophenyl)pyrrolidine exhibits significant biological activity, particularly in the context of drug development. Its interaction with specific molecular targets, such as enzymes or receptors, suggests potential therapeutic applications. The compound's ability to modulate biological pathways makes it a candidate for further investigation in pharmacology.