structure of 2-Chloro-n-(5-acetamido-2-methoxyphenyl)propanamide

2-Chloro-n-(5-acetamido-2-methoxyphenyl)propanamide

CAS No.: 1000930-64-2
M. Wt: 270.71
M. Fa: C12H15ClN2O3
InChI Key: LIGDNBXHAHYSCZ-UHFFFAOYSA-N

Names and Identifiers of 1000930-64-2

CAS Number

1000930-64-2

MDL Number

MFCD09971334

IUPAC Name

2-chloro-N-(5-acetamido-2-methoxyphenyl)propanamide

InChI

InChI=1S/C12H15ClN2O3/c1-7(13)12(17)15-10-6-9(14-8(2)16)4-5-11(10)18-3/h4-7H,1-3H3,(H,14,16)(H,15,17)

InChIKey

LIGDNBXHAHYSCZ-UHFFFAOYSA-N

Canonical SMILES

COC1=CC=C(NC(C)=O)C=C1NC(=O)C(C)Cl

UNSPSC Code

12352100

Physical and chemical properties of 1000930-64-2

Acidity coefficient

12.10±0.70(Predicted)

Boiling Point

488.8±45.0 °C(Predicted)

Density

1.302±0.06 g/cm3(Predicted)

H Bond Acceptors

3

H Bond Donors

2

LogP

1.39710333733333

Molecular Formula

C12H15ClN2O3

Molecular Weight

270.71

Safety Information of 1000930-64-2

Pictograms

Signal Word

 Warning

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

Applications of 1000930-64-2

2-chloro-N-(5-acetamido-2-methoxyphenyl)propanamide finds applications in various fields:

  • Organic Chemistry: As a reagent in organic synthesis and as a building block for more complex molecules.
  • Biological Research: In studies focusing on enzyme inhibition and protein interactions.
  • Pharmaceutical Industry: Used in the synthesis of specialty chemicals and materials relevant to drug development.

Interaction Studies of 1000930-64-2

Research into the interactions of 2-chloro-N-(5-acetamido-2-methoxyphenyl)propanamide with biological molecules reveals its potential to affect enzyme activity and receptor binding. The unique combination of functional groups enhances its ability to form hydrogen bonds and engage in other molecular interactions, which may lead to significant biological effects.

Biological Activity of 1000930-64-2

The biological activity of 2-chloro-N-(5-acetamido-2-methoxyphenyl)propanamide is significant in research involving enzyme inhibition and protein interactions. The compound's structure allows it to engage with specific molecular targets, potentially modulating enzymatic activities or receptor functions. This makes it valuable in pharmacological studies aimed at understanding disease mechanisms or developing therapeutic agents.