structure of (5-Ethyl-1,3-thiazol-2-yl)methanamine

(5-Ethyl-1,3-thiazol-2-yl)methanamine

CAS No.: 1017435-71-0
M. Wt: 142.22
M. Fa: C6H10N2S
InChI Key: RXAXYPLDNOJHNJ-UHFFFAOYSA-N

Names and Identifiers of (5-Ethyl-1,3-thiazol-2-yl)methanamine

CAS Number

1017435-71-0

EC Number

871-851-0

MDL Number

MFCD09904507

IUPAC Name

(5-ethyl-1,3-thiazol-2-yl)methanamine

InChI

InChI=1S/C6H10N2S/c1-2-5-4-8-6(3-7)9-5/h4H,2-3,7H2,1H3

InChIKey

RXAXYPLDNOJHNJ-UHFFFAOYSA-N

Canonical SMILES

CCC1=CN=C(S1)CN

UNSPSC Code

12352100

Physical and chemical properties of (5-Ethyl-1,3-thiazol-2-yl)methanamine

Acidity coefficient

7.53±0.29(Predicted)

Boiling Point

218.6±23.0 °C(Predicted)

Density

1.138±0.06 g/cm3(Predicted)

H Bond Acceptors

2

H Bond Donors

1

LogP

0.921402958666667

Molecular Formula

C6H10N2S

Molecular Weight

142.22

Safety Information of (5-Ethyl-1,3-thiazol-2-yl)methanamine

Pictograms

Signal Word

 Danger

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

Applications of (5-Ethyl-1,3-thiazol-2-yl)methanamine

(5-Ethyl-1,3-thiazol-2-yl)methanamine finds applications primarily in:

  • Medicinal chemistry: As a building block for synthesizing new pharmaceutical agents.
  • Research: In studies exploring thiazole derivatives and their biological implications.
  • Agricultural chemistry: Potentially as a component in agrochemicals due to its biological activity.

Interaction Studies of (5-Ethyl-1,3-thiazol-2-yl)methanamine

Interaction studies involving (5-Ethyl-1,3-thiazol-2-yl)methanamine have focused on its binding affinity with various biological targets. Preliminary data suggest that it may interact with enzymes or receptors relevant to disease pathways, indicating its potential as a lead compound in drug discovery.

Biological Activity of (5-Ethyl-1,3-thiazol-2-yl)methanamine

Research indicates that (5-Ethyl-1,3-thiazol-2-yl)methanamine exhibits notable biological activities. It has been studied for its potential antimicrobial properties and as a precursor to various biologically active compounds. The thiazole moiety is often associated with pharmacological effects, making this compound of interest for drug development.