Cas no 148148-45-2 (2,5-dimethoxy-N,N-dimethylbenzene-1-sulfonamide)

2,5-Dimethoxy-N,N-dimethylbenzene-1-sulfonamide is a sulfonamide derivative characterized by its dimethyl-substituted benzene ring with methoxy groups at the 2- and 5-positions. This compound is of interest in synthetic organic chemistry due to its potential as an intermediate in the preparation of more complex molecules, particularly in pharmaceutical and agrochemical research. The electron-donating methoxy and dimethylamino groups enhance its reactivity in electrophilic aromatic substitution and other transformations. Its well-defined structure and stability under standard conditions make it a reliable building block for further functionalization. The compound's solubility in common organic solvents further facilitates its use in laboratory-scale reactions.
2,5-dimethoxy-N,N-dimethylbenzene-1-sulfonamide structure
148148-45-2 structure
Product Name:2,5-dimethoxy-N,N-dimethylbenzene-1-sulfonamide
CAS No:148148-45-2
MF:C10H15NO4S
MW:245.2954018116
CID:1319595
PubChem ID:8441929
Update Time:2025-08-05

2,5-dimethoxy-N,N-dimethylbenzene-1-sulfonamide Chemical and Physical Properties

Names and Identifiers

    • Benzenesulfonamide, 2,5-dimethoxy-N,N-dimethyl-
    • 2,5-dimethoxy-N,N-dimethylbenzene-1-sulfonamide
    • Z45527640
    • AKOS001429642
    • 148148-45-2
    • F1657-1714
    • SCHEMBL8602441
    • 2,5-dimethoxy-N,N-dimethylbenzenesulfonamide
    • 2,5-dimethoxy-n,n-dimethyl-benzenesulfonamide
    • Inchi: 1S/C10H15NO4S/c1-11(2)16(12,13)10-7-8(14-3)5-6-9(10)15-4/h5-7H,1-4H3
    • InChI Key: SONMTGIQVOUWTG-UHFFFAOYSA-N
    • SMILES: S(C1C=C(C=CC=1OC)OC)(N(C)C)(=O)=O

Computed Properties

  • Exact Mass: 245.07225
  • Monoisotopic Mass: 245.07217913g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 4
  • Complexity: 309
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1
  • Topological Polar Surface Area: 64.2?2

Experimental Properties

  • PSA: 55.84

2,5-dimethoxy-N,N-dimethylbenzene-1-sulfonamide Pricemore >>

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Additional information on 2,5-dimethoxy-N,N-dimethylbenzene-1-sulfonamide

2,5-Dimethoxy-N,N-Dimethylbenzene-1-Sulfonamide: A Comprehensive Overview

The compound 2,5-dimethoxy-N,N-dimethylbenzene-1-sulfonamide (CAS No. 148148-45-2) is a highly specialized organic compound with a unique structure and diverse applications. This compound belongs to the class of sulfonamides, which are widely used in pharmaceuticals, agrochemicals, and materials science. The molecule consists of a benzene ring substituted with two methoxy groups at the 2 and 5 positions, a sulfonamide group at the 1 position, and two methyl groups attached to the nitrogen atom of the sulfonamide. This specific substitution pattern imparts distinctive chemical and physical properties to the compound.

Recent studies have highlighted the potential of 2,5-dimethoxy-N,N-dimethylbenzene-1-sulfonamide in various fields. For instance, researchers have explored its role as an intermediate in the synthesis of bioactive compounds. The methoxy groups at positions 2 and 5 contribute to the molecule's electronic properties, making it a versatile building block for drug discovery. Additionally, the sulfonamide group is known for its ability to form hydrogen bonds, which is crucial in designing molecules with specific biological activities.

The synthesis of 2,5-dimethoxy-N,N-dimethylbenzene-1-sulfonamide typically involves multi-step reactions. One common approach includes the sulfonation of a dimethoxybenzene derivative followed by nucleophilic substitution to introduce the sulfonamide group. The reaction conditions are carefully optimized to ensure high yields and purity. Recent advancements in catalytic methods have further enhanced the efficiency of these reactions, making the compound more accessible for large-scale production.

In terms of applications, 2,5-dimethoxy-N,N-dimethylbenzene-1-sulfonamide has shown promise in the development of herbicides and fungicides. Its ability to inhibit key enzymes in plant pathogens makes it a valuable candidate for agricultural chemicals. Furthermore, studies have demonstrated its potential as a stabilizer in polymer materials due to its ability to form strong intermolecular interactions.

From an environmental perspective, understanding the fate and transport of 2,5-dimethoxy-N,N-dimethylbenzene-1-sulfonamide is critical for its safe use. Research indicates that the compound undergoes biodegradation under certain conditions, reducing its persistence in the environment. However, further studies are needed to assess its long-term impact on ecosystems.

In conclusion, 2,5-dimethoxy-N,N-dimethylbenzene-1-sulfonamide (CAS No. 148148-45-2) is a multifaceted compound with significant potential in various industries. Its unique structure and reactivity make it an essential component in modern chemical synthesis and application development.

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