Cas no 620103-27-7 (2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid)

2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid is a specialized organic compound featuring a morpholine sulfonyl group and a carboxylic acid functionality. Its structure incorporates a phenyl ring substituted with a sulfonamide linkage to morpholine, enhancing its potential as an intermediate in pharmaceutical synthesis or biochemical research. The presence of both amide and carboxyl groups offers versatility in further derivatization, making it valuable for drug design, particularly in targeting enzyme inhibition or receptor modulation. The compound’s well-defined molecular architecture ensures consistent reactivity, while its polar groups contribute to solubility in common organic solvents, facilitating handling in synthetic applications. Its structural features suggest utility in medicinal chemistry for developing bioactive molecules.
2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid structure
620103-27-7 structure
Product Name:2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid
CAS No:620103-27-7
MF:C14H18N2O6S
MW:342.367522716522
MDL:MFCD03723713
CID:3143339
PubChem ID:2050012
Update Time:2025-10-18

2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid Chemical and Physical Properties

Names and Identifiers

    • 2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid
    • DA-56216
    • AB00677685-01
    • F1924-0005
    • C14H18N2O6S
    • 620103-27-7
    • EN300-236432
    • 2-[methyl-(4-morpholin-4-ylsulfonylbenzoyl)amino]acetic Acid
    • HY-W027581
    • AKOS002727309
    • N-Methyl-N-[4-(morpholin-4-ylsulfonyl)benzoyl]glycine
    • CS-0071605
    • MDL: MFCD03723713
    • Inchi: 1S/C14H18N2O6S/c1-15(10-13(17)18)14(19)11-2-4-12(5-3-11)23(20,21)16-6-8-22-9-7-16/h2-5H,6-10H2,1H3,(H,17,18)
    • InChI Key: UFOXZFIVYHTHDZ-UHFFFAOYSA-N
    • SMILES: S(C1C=CC(C(N(C)CC(=O)O)=O)=CC=1)(N1CCOCC1)(=O)=O

Computed Properties

  • Exact Mass: 342.08855747g/mol
  • Monoisotopic Mass: 342.08855747g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 7
  • Heavy Atom Count: 23
  • Rotatable Bond Count: 5
  • Complexity: 530
  • 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: -0.2
  • Topological Polar Surface Area: 113?2

2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid Pricemore >>

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Additional information on 2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid

Comprehensive Overview of 2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid (CAS No. 620103-27-7)

2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid (CAS No. 620103-27-7) is a specialized organic compound that has garnered significant attention in pharmaceutical and biochemical research due to its unique structural features and potential applications. This compound, often referred to by its CAS number 620103-27-7, belongs to a class of sulfonamide derivatives, which are widely studied for their bioactive properties. The presence of both morpholine and sulfonyl groups in its structure makes it a promising candidate for drug discovery and development.

One of the key reasons for the growing interest in 2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid is its potential role in modulating enzyme activity. Researchers have explored its interactions with various biological targets, particularly those involved in inflammatory pathways. The compound's N-methyl and acetic acid moieties contribute to its solubility and bioavailability, which are critical factors in drug design. Additionally, the morpholine-4-sulfonyl group enhances its ability to bind to specific protein sites, making it a valuable tool for studying signal transduction mechanisms.

In recent years, the demand for sulfonamide-based compounds has surged, driven by their applications in treating a range of conditions. 2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid is no exception, as it has been investigated for its potential anti-inflammatory and antimicrobial properties. These studies align with current trends in precision medicine, where researchers seek to develop targeted therapies with minimal side effects. The compound's CAS number 620103-27-7 is frequently searched in academic databases, reflecting its relevance in ongoing research.

The synthesis of 2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid involves multi-step organic reactions, including sulfonylation and amidation. These processes require careful optimization to ensure high yield and purity, which are essential for its use in biological assays. The compound's morpholine ring is particularly noteworthy, as it is a common pharmacophore in many FDA-approved drugs. This structural feature has led to speculation about its potential as a scaffold for developing new therapeutics.

From an industrial perspective, CAS No. 620103-27-7 is often discussed in the context of green chemistry and sustainable synthesis. Researchers are exploring eco-friendly methods to produce this compound, such as catalytic reactions and solvent-free conditions. These efforts resonate with the global push toward environmentally responsible practices in chemical manufacturing. The compound's acetic acid group also makes it amenable to further derivatization, opening doors for the creation of novel analogs with enhanced properties.

In summary, 2-{N-methyl-1-[4-(morpholine-4-sulfonyl)phenyl]formamido}acetic acid (CAS No. 620103-27-7) represents a fascinating area of study at the intersection of chemistry and biology. Its unique structure, combined with its potential therapeutic applications, makes it a subject of ongoing research. As the scientific community continues to uncover its mechanisms of action, this compound may pave the way for innovative treatments in the years to come.

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