CAS 339-44-6

Benzenesulfonamide, N-[5-(2-methoxyethoxy)-2-pyrimidinyl]-

Description:

Benzenesulfonamide, N-[5-(2-methoxyethoxy)-2-pyrimidinyl]- is a chemical compound characterized by its sulfonamide functional group, which is known for its antibacterial properties. This compound features a pyrimidine ring substituted with a 2-methoxyethoxy group, contributing to its solubility and potential biological activity. The presence of the benzenesulfonamide moiety suggests that it may interact with various biological targets, making it of interest in medicinal chemistry. The compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its molecular structure allows for hydrogen bonding and potential interactions with proteins, which can influence its pharmacological properties. Additionally, the methoxyethoxy group enhances its lipophilicity, potentially affecting its absorption and distribution in biological systems. Overall, this compound's unique structure and functional groups position it as a candidate for further research in drug development and therapeutic applications.

Formula: C₁₃H₁₅N₃O₄S

InChI: InChI=1/C13H15N3O4S/c1-19-7-8-20-11-9-14-13(15-10-11)16-21(17,18)12-5-3-2-4-6-12/h2-6,9-10H,7-8H2,1H3,(H,14,15,16)

InChI key: InChIKey=QFWPJPIVLCBXFJ-UHFFFAOYSA-N

SMILES: S(NC=1N=CC(OCCOC)=CN1)(=O)(=O)C2=CC=CC=C2

Synonyms:

• 2-Benzenesulfonamido-5-(2-methoxyethoxy)pyrimidine
• Glidiazine
• Glymidine
• N-[5-(2-Methoxyethoxy)-2-pyrimidinyl]benzolsulfonamid
• N-[5-(2-methoxyethoxy)-2-pyrimidinyl]benzenesulfonamide
• N-[5-(2-methoxyethoxy)-2-pyrimidinyl]benzenesulphonamide
• N-[5-(2-metoxietoxi)-2-pirimidinil]bencenosulfonamida
• Glycodiazin
• Benzenesulfonamide, N-[5-(2-methoxyethoxy)-2-pyrimidinyl]-
• 2-Benzolsulfonamido-5-beta-methoxy-aethoxy-pyrimidine
• BRN 0552655
• 5-beta-(Methoxyethoxy)-2-(phenylsulfonylamido)pyrimidine
• Benzenesulfonamide, N-(5-(2-methoxyethoxy)-2-pyrimidinyl)-
• Glymidinum
• UNII-4C5I4BQZ8F
• 5-25-12-00549 (Beilstein Handbook Reference)
• Glycodiazin [German]
• 2-Benzolsulfonamido-5-beta-methoxy-aethoxy-pyrimidine [German]
• Glycodiazine

Glymidine

CAS: 339-44-6

Glycodiazine, a sulfadiazine derivative, reduces blood sugar by boosting insulin release and sensitivity.

Formula: C₁₃H₁₅N₃O₄S

Color and Shape: Solid

Molecular weight: 309.34

Ref: TM-T31960

Glymidine

Controlled Product

CAS: 339-44-6

Applications Glymidine is used in biological activities to predict human intestinal absorption in drug discovery.
References Moda, T. L. et al.: Bioorg. Med. Chem. Lett., 22, 2889 (2012);

Formula: C₁₃H₁₅N₃O₄S

Color and Shape: Neat

Molecular weight: 309.34

Ref: TR-G752000

Glymidine-d5

Controlled Product

CAS: 339-44-6

Formula: C₁₃D₅H₁₀N₃O₄S

Color and Shape: Neat

Molecular weight: 314.372

Ref: TR-G752002