structure of 3-(5-chlorothiophen-2-yl)propan-1-amine

3-(5-chlorothiophen-2-yl)propan-1-amine

CAS No.: 1000564-79-3
M. Wt: 175.68
M. Fa: C7H10ClNS
InChI Key: QLTBPZNOWOEBDH-UHFFFAOYSA-N

Names and Identifiers of 3-(5-chlorothiophen-2-yl)propan-1-amine

CAS Number

1000564-79-3

MDL Number

MFCD09913007

IUPAC Name

3-(5-chlorothiophen-2-yl)propan-1-amine

InChI

InChI=1S/C7H10ClNS/c8-7-4-3-6(10-7)2-1-5-9/h3-4H,1-2,5,9H2

InChIKey

QLTBPZNOWOEBDH-UHFFFAOYSA-N

Canonical SMILES

NCCCC1=CC=C(Cl)S1

UNSPSC Code

12352100

Physical and chemical properties of 3-(5-chlorothiophen-2-yl)propan-1-amine

Acidity coefficient

9.90±0.10(Predicted)

Boiling Point

245.8±30.0 °C(Predicted)

Density

1?+-.0.06 g/cm3(Predicted)

H Bond Acceptors

1

H Bond Donors

1

LogP

2.515166143

Molecular Formula

C7H10ClNS

Molecular Weight

175.68

Safety Information of 3-(5-chlorothiophen-2-yl)propan-1-amine

Pictograms

Signal Word

 Warning

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

Applications of 3-(5-chlorothiophen-2-yl)propan-1-amine

3-(5-Chlorothiophen-2-yl)propan-1-amine has several applications across various fields:

  • Chemistry: Used as an intermediate in the synthesis of more complex organic molecules.
  • Biology: Studied for its potential biological activities, including antimicrobial and anticancer properties.
  • Medicine: Research is ongoing to explore its potential as a pharmaceutical agent.
  • Industry: Utilized in developing materials such as organic semiconductors and corrosion inhibitors.

Interaction Studies of 3-(5-chlorothiophen-2-yl)propan-1-amine

The interaction studies of 3-(5-Chlorothiophen-2-yl)propan-1-amine focus on its binding affinity to specific enzymes and receptors. These studies are crucial for understanding its mechanism of action and potential therapeutic applications. The exact pathways and targets are subjects of ongoing research, contributing valuable insights into its biological activity.

Biological Activity of 3-(5-chlorothiophen-2-yl)propan-1-amine

Research indicates that 3-(5-Chlorothiophen-2-yl)propan-1-amine exhibits potential biological activities, particularly in antimicrobial and anticancer domains. Its interactions with specific molecular targets suggest that it may modulate enzyme or receptor activity, leading to various biological effects. Ongoing studies aim to elucidate its mechanisms of action and therapeutic potential.