Cas no 670255-96-6 (N-(2,4-Dimethylphenyl)sulfonylglycine)

N-(2,4-Dimethylphenyl)sulfonylglycine is a sulfonamide derivative with applications in organic synthesis and pharmaceutical research. Its structure features a glycine moiety linked to a 2,4-dimethylphenylsulfonyl group, offering reactivity for further functionalization. The compound is valued for its potential as an intermediate in the development of bioactive molecules, including enzyme inhibitors or prodrugs. Its sulfonamide group enhances stability and solubility, while the aromatic dimethyl substitution may influence steric and electronic properties. Suitable for controlled reactions, it is typically handled under standard laboratory conditions. Purity and consistency are critical for reproducible results in research applications. Proper storage in a cool, dry environment is recommended to maintain stability.
N-(2,4-Dimethylphenyl)sulfonylglycine structure
670255-96-6 structure
Product Name:N-(2,4-Dimethylphenyl)sulfonylglycine
CAS No:670255-96-6
MF:C10H13NO4S
MW:243.27952170372
MDL:MFCD05986314
CID:965203
PubChem ID:2196273
Update Time:2025-10-18

N-(2,4-Dimethylphenyl)sulfonylglycine Chemical and Physical Properties

Names and Identifiers

    • 2-(2,4-Dimethylphenylsulfonamido)acetic acid
    • [[(2,4-DIMETHYLPHENYL)SULFONYL]AMINO]ACETIC ACID
    • {[(2,4-dimethylphenyl)sulfonyl]amino}acetic acid
    • 2-[(2,4-dimethylphenyl)sulfonylamino]acetic acid
    • N-[(2,4-dimethylphenyl)sulfonyl]glycine(SALTDATA: FREE)
    • AC1M3T2H
    • AC1Q2HY8
    • AQ-390
    • CBKinase1_004118
    • CBKinase1_016518
    • CTK5C5577
    • N-[(2,4-dimethylphenyl)sulfonyl]glycine
    • ([(2,4-DIMETHYLPHENYL)SULFONYL]AMINO)ACETIC ACID
    • SR-01000268304-1
    • D95038
    • SR-01000268304
    • AKOS002384039
    • 2-(2,4-Dimethylphenylsulfonamido)aceticacid
    • MFCD05986314
    • BRD-K22260652-001-01-8
    • EN300-86941
    • CS-0153315
    • 2-(2,4-dimethylbenzenesulfonamido)acetic acid
    • DTXSID20366938
    • 670255-96-6
    • AQ-390/42119913
    • BS-38409
    • ((2,4-dimethylphenyl)sulfonylamino)acetic acid
    • N-(2,4-Dimethylbenzene-1-sulfonyl)glycine
    • DB-199003
    • (2,4-DIMETHYLBENZENESULFONAMIDO)ACETIC ACID
    • N-(2,4-Dimethylphenyl)sulfonylglycine
    • MDL: MFCD05986314
    • Inchi: 1S/C10H13NO4S/c1-7-3-4-9(8(2)5-7)16(14,15)11-6-10(12)13/h3-5,11H,6H2,1-2H3,(H,12,13)
    • InChI Key: QXSZBHFZFCHZEJ-UHFFFAOYSA-N
    • SMILES: S(C1C=CC(C)=CC=1C)(NCC(=O)O)(=O)=O

Computed Properties

  • Exact Mass: 243.05700
  • Monoisotopic Mass: 243.05652907g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 4
  • Complexity: 346
  • 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: 1.2
  • Topological Polar Surface Area: 91.8?2

Experimental Properties

  • Density: 1.324
  • Boiling Point: 440.7°C at 760 mmHg
  • Flash Point: 220.3°C
  • Refractive Index: 1.559
  • PSA: 91.85000
  • LogP: 2.13800

N-(2,4-Dimethylphenyl)sulfonylglycine 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%

N-(2,4-Dimethylphenyl)sulfonylglycine Pricemore >>

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Additional information on N-(2,4-Dimethylphenyl)sulfonylglycine

Research Brief on N-(2,4-Dimethylphenyl)sulfonylglycine (CAS: 670255-96-6): Recent Advances and Applications

N-(2,4-Dimethylphenyl)sulfonylglycine (CAS: 670255-96-6) is a sulfonamide derivative that has garnered significant attention in the field of chemical biology and medicinal chemistry due to its potential therapeutic applications. Recent studies have explored its role as a key intermediate in the synthesis of bioactive compounds, particularly in the development of enzyme inhibitors and anti-inflammatory agents. This research brief consolidates the latest findings on this compound, highlighting its chemical properties, biological activities, and emerging applications in drug discovery.

One of the most notable advancements in the study of N-(2,4-Dimethylphenyl)sulfonylglycine is its application in the design of matrix metalloproteinase (MMP) inhibitors. MMPs are a family of zinc-dependent endopeptidases implicated in various pathological conditions, including cancer metastasis and inflammatory diseases. A 2023 study published in the Journal of Medicinal Chemistry demonstrated that derivatives of N-(2,4-Dimethylphenyl)sulfonylglycine exhibit potent inhibitory activity against MMP-2 and MMP-9, with IC50 values in the nanomolar range. The study utilized molecular docking and kinetic assays to elucidate the binding interactions, revealing a strong affinity for the zinc-binding domain of these enzymes.

In addition to its role in MMP inhibition, N-(2,4-Dimethylphenyl)sulfonylglycine has been investigated for its anti-inflammatory properties. A recent preclinical study published in Bioorganic & Medicinal Chemistry Letters reported that this compound significantly reduces the production of pro-inflammatory cytokines, such as TNF-α and IL-6, in macrophage cell lines. The study attributed this effect to the compound's ability to modulate the NF-κB signaling pathway, suggesting its potential as a lead compound for developing novel anti-inflammatory therapeutics.

From a synthetic chemistry perspective, N-(2,4-Dimethylphenyl)sulfonylglycine serves as a versatile building block for the preparation of sulfonamide-based drugs. A 2022 study in Organic & Biomolecular Chemistry detailed an efficient, one-pot synthesis method for this compound, employing green chemistry principles to minimize environmental impact. The optimized protocol achieved a high yield (85%) and purity (>98%), making it suitable for large-scale pharmaceutical production.

Despite these promising developments, challenges remain in the clinical translation of N-(2,4-Dimethylphenyl)sulfonylglycine-based therapeutics. Pharmacokinetic studies indicate that the compound exhibits moderate bioavailability and requires further structural optimization to enhance its metabolic stability. Ongoing research is focused on designing prodrugs and nanoformulations to address these limitations, as highlighted in a 2023 review article in Advanced Drug Delivery Reviews.

In conclusion, N-(2,4-Dimethylphenyl)sulfonylglycine (CAS: 670255-96-6) represents a promising scaffold for drug discovery, with demonstrated applications in enzyme inhibition and anti-inflammatory therapy. Continued research into its mechanism of action and drug delivery strategies will be critical for advancing its therapeutic potential. This brief underscores the importance of interdisciplinary collaboration in translating chemical discoveries into clinically viable treatments.

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