structure of ({6-chloroimidazo[2,1-b][1,3]thiazol-5-yl}methyl)(methyl)amine

({6-chloroimidazo[2,1-b][1,3]thiazol-5-yl}methyl)(methyl)amine

CAS No.: 1000930-88-0
M. Wt: 201.68
M. Fa: C7H8ClN3S
InChI Key: VOTYHCIVROFUSU-UHFFFAOYSA-N

Names and Identifiers of 1000930-88-0

CAS Number

1000930-88-0

MDL Number

MFCD09802072

IUPAC Name

({6-chloroimidazo[2,1-b][1,3]thiazol-5-yl}methyl)(methyl)amine

InChI

InChI=1S/C7H8ClN3S/c1-9-4-5-6(8)10-7-11(5)2-3-12-7/h2-3,9H,4H2,1H3

InChIKey

VOTYHCIVROFUSU-UHFFFAOYSA-N

Canonical SMILES

CNCC1=C(Cl)N=C2SC=CN21

UNSPSC Code

12352100

Physical and chemical properties of 1000930-88-0

H Bond Acceptors

2

H Bond Donors

1

LogP

1.095822549

Molecular Formula

C7H8ClN3S

Molecular Weight

201.68

Safety Information of 1000930-88-0

Pictograms

Signal Word

 Warning

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

Applications of 1000930-88-0

The applications of ({6-Chloroimidazo[2,1-b][1,3]thiazol-5-yl}methyl)(methyl)amine are diverse:

  • Pharmaceutical Development: It serves as a building block in synthesizing new drugs targeting various diseases.
  • Biochemical Research: The compound is utilized in studies exploring enzyme interactions and metabolic pathways.
  • Agricultural Chemistry: Potential applications in developing agrochemicals aimed at pest control are also being investigated.

Interaction Studies of 1000930-88-0

Studies on the interactions of this compound with biological targets are crucial for understanding its pharmacological potential. Research has focused on:

  • Binding Affinity Studies: Assessing how well the compound binds to specific receptors or enzymes.
  • Mechanistic Studies: Investigating how the compound influences biological pathways at a molecular level.

These studies provide insights into optimizing the compound for therapeutic use.

Biological Activity of 1000930-88-0

Research indicates that compounds containing imidazole and thiazole moieties often exhibit significant biological activities. Specifically, ({6-Chloroimidazo[2,1-b][1,3]thiazol-5-yl}methyl)(methyl)amine has been studied for its potential:

  • Antimicrobial Activity: Some studies suggest that derivatives of this compound may possess antimicrobial properties against various pathogens.
  • Anticancer Activity: There is ongoing research into its efficacy as an anticancer agent due to its ability to interfere with cellular mechanisms involved in tumor growth.
  • Enzyme Inhibition: The compound may also act as an inhibitor for specific enzymes, making it a candidate for drug development targeting metabolic pathways.