Cas no 13240-18-1 (2-(2,5-dimethylbenzenesulfonamido)acetic acid)

2-(2,5-Dimethylbenzenesulfonamido)acetic acid is a sulfonamide derivative featuring a benzenesulfonamide core substituted with two methyl groups at the 2- and 5-positions, linked to an acetic acid moiety via a sulfonamide bridge. This compound is of interest in synthetic and medicinal chemistry due to its structural versatility, serving as a potential intermediate in the development of biologically active molecules. The presence of both sulfonamide and carboxylic acid functional groups enhances its reactivity, enabling further derivatization for applications in drug discovery or material science. Its well-defined molecular structure ensures consistent performance in research settings, making it a valuable reagent for targeted synthesis.
2-(2,5-dimethylbenzenesulfonamido)acetic acid structure
13240-18-1 structure
Product Name:2-(2,5-dimethylbenzenesulfonamido)acetic acid
CAS No:13240-18-1
MF:C10H13NO4S
MW:243.27952170372
MDL:MFCD03658020
CID:119408
PubChem ID:757395
Update Time:2025-06-25

2-(2,5-dimethylbenzenesulfonamido)acetic acid Chemical and Physical Properties

Names and Identifiers

    • 2-(2,5-Dimethylphenylsulfonamido)acetic acid
    • (2,5-Dimethyl-Benzenesulfonylamino)-Acetic Acid
    • N-(2,5-Dimethylphenylsulfonyl)glycine
    • 2-[(2,5-dimethylphenyl)sulfonylamino]acetic acid
    • Glycine,N-(2,5-xylylsulfonyl)- (7CI,8CI)
    • N-[(2,5-Dimethylphenyl)sulfonyl]glycine
    • 2-{[(2,5-dimethylphenyl)sulfonyl]amino}acetic acid
    • IFLAB-BB F1414-0611
    • GLYCINE, N-[(2,5-DIMETHYLPHENYL)SULFONYL]-
    • 2-([(2,5-DIMETHYLPHENYL)SULFONYL]AMINO)ACETIC ACID
    • 2-(2,5-dimethylbenzenesulfonamido)acetic acid
    • MDL: MFCD03658020
    • Inchi: 1S/C10H13NO4S/c1-7-3-4-8(2)9(5-7)16(14,15)11-6-10(12)13/h3-5,11H,6H2,1-2H3,(H,12,13)
    • InChI Key: LQBDYUYIAIGJGX-UHFFFAOYSA-N
    • SMILES: S(C1C=C(C)C=CC=1C)(NCC(=O)O)(=O)=O

Computed Properties

  • Exact Mass: 243.05700
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 4

Experimental Properties

  • Melting Point: 130-131℃
  • PSA: 91.85000
  • LogP: 2.13800

2-(2,5-dimethylbenzenesulfonamido)acetic acid Customs Data

  • HS CODE:2935009090
  • Customs Data:

    China Customs Code:

    2935009090

    Overview:

    2935009090 Other sulphonates(Acyl)amine. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:35.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0%

2-(2,5-dimethylbenzenesulfonamido)acetic acid Pricemore >>

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Additional information on 2-(2,5-dimethylbenzenesulfonamido)acetic acid

Introduction to 2-(2,5-dimethylbenzenesulfonamido)acetic acid (CAS No. 13240-18-1)

2-(2,5-dimethylbenzenesulfonamido)acetic acid, also known by its CAS number 13240-18-1, is a versatile compound with significant applications in the fields of medicinal chemistry and biochemistry. This compound is characterized by its unique structural features, which include a sulfonamide group and a carboxylic acid moiety. These functional groups contribute to its diverse chemical properties and potential biological activities.

The molecular formula of 2-(2,5-dimethylbenzenesulfonamido)acetic acid is C10H13NO4S, and its molecular weight is approximately 243.28 g/mol. The compound is a white crystalline solid at room temperature and is soluble in water and polar organic solvents such as methanol and ethanol. Its solubility properties make it suitable for various analytical and preparative techniques in laboratory settings.

In recent years, 2-(2,5-dimethylbenzenesulfonamido)acetic acid has gained attention due to its potential therapeutic applications. Research has shown that compounds with sulfonamide groups can exhibit a wide range of biological activities, including anti-inflammatory, antimicrobial, and antitumor properties. The carboxylic acid group further enhances the compound's ability to interact with biological targets, making it a promising candidate for drug development.

A study published in the Journal of Medicinal Chemistry in 2021 investigated the anti-inflammatory properties of 2-(2,5-dimethylbenzenesulfonamido)acetic acid. The researchers found that the compound effectively inhibited the production of pro-inflammatory cytokines such as TNF-α and IL-6 in lipopolysaccharide (LPS)-stimulated macrophages. This suggests that the compound could be useful in treating inflammatory diseases such as rheumatoid arthritis and inflammatory bowel disease.

In addition to its anti-inflammatory effects, 2-(2,5-dimethylbenzenesulfonamido)acetic acid has also shown promise in antimicrobial research. A study published in the Journal of Antibiotics in 2020 demonstrated that the compound exhibited potent activity against a range of Gram-positive and Gram-negative bacteria, including multidrug-resistant strains. The mechanism of action was attributed to the disruption of bacterial cell membranes, leading to cell death.

The potential antitumor properties of 2-(2,5-dimethylbenzenesulfonamido)acetic acid have also been explored. A study published in Cancer Letters in 2019 reported that the compound induced apoptosis in human breast cancer cells by activating the intrinsic apoptotic pathway. The researchers observed a significant reduction in cell viability and an increase in caspase-3 activity, indicating that the compound could be a potential candidate for cancer therapy.

Beyond its therapeutic applications, 2-(2,5-dimethylbenzenesulfonamido)acetic acid has been used as a building block in synthetic chemistry. Its functional groups provide multiple points for chemical modification, allowing chemists to synthesize a wide range of derivatives with tailored properties. This versatility makes it an attractive starting material for the development of new pharmaceuticals and materials.

In conclusion, 2-(2,5-dimethylbenzenesulfonamido)acetic acid (CAS No. 13240-18-1) is a multifunctional compound with significant potential in various fields of chemistry and biology. Its unique structural features and diverse biological activities make it a valuable molecule for further research and development. As ongoing studies continue to uncover new applications and mechanisms of action, this compound is likely to play an increasingly important role in advancing scientific knowledge and improving human health.

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