structure of N-Ethyl-N-(4-methoxybenzyl)benzenesulphonamide

N-Ethyl-N-(4-methoxybenzyl)benzenesulphonamide

CAS No.: 1000339-36-5
M. Wt: 305.39200
M. Fa: C16H19NO3S
InChI Key: FPJRJXFBGCSTSH-UHFFFAOYSA-N

Names and Identifiers of 1000339-36-5

CAS Number

1000339-36-5

MDL Number

MFCD09878415

IUPAC Name

N-ethyl-N-[(4-methoxyphenyl)methyl]benzenesulfonamide

InChI

InChI=1S/C16H19NO3S/c1-3-17(13-14-9-11-15(20-2)12-10-14)21(18,19)16-7-5-4-6-8-16/h4-12H,3,13H2,1-2H3

InChIKey

FPJRJXFBGCSTSH-UHFFFAOYSA-N

Canonical SMILES

CCN(CC1=CC=C(OC)C=C1)S(=O)(=O)C1=CC=CC=C1

UNSPSC Code

12352100

Physical and chemical properties of 1000339-36-5

Exact Mass

305.10900

H Bond Acceptors

3

H Bond Donors

0

LogP

3.98680

Molecular Formula

C16H19NO3S

Molecular Weight

305.39200

PSA

54.99000

Safety Information of 1000339-36-5

Pictograms

Signal Word

 Warning

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

Applications of 1000339-36-5

N-Ethyl-N-(4-methoxybenzyl)benzenesulfonamide has potential applications in various fields:

  • Pharmaceuticals: Due to its biological activity, it may serve as a lead compound for developing new antimicrobial or antiviral drugs.
  • Chemical Research: It can be used as a building block in organic synthesis for creating more complex molecules.
  • Agricultural Chemicals: Its properties may be explored for use in developing agrochemicals.

Interaction Studies of 1000339-36-5

Studies investigating the interactions of N-Ethyl-N-(4-methoxybenzyl)benzenesulfonamide with biological targets have shown that:

  • The compound can interact with specific enzymes involved in metabolic pathways, potentially leading to inhibition or modulation of these pathways.
  • Structure-activity relationship (SAR) studies highlight how variations in substituents affect binding affinity and biological efficacy.

Biological Activity of 1000339-36-5

Benzenesulfonamides, including N-Ethyl-N-(4-methoxybenzyl)benzenesulfonamide, exhibit a range of biological activities:

  • Antimicrobial Properties: Many sulfonamides are known for their antibacterial effects, particularly against Gram-positive bacteria.
  • Antiviral Activity: Research indicates that modifications in the structure of benzenesulfonamides can enhance their antiviral properties, making them potential candidates for treating viral infections.
  • Carbonic Anhydrase Inhibition: Some derivatives have shown promise as inhibitors of carbonic anhydrase, which is relevant in treating conditions like glaucoma and epilepsy.