CymitQuimica logo

CAS 64398-84-1

:

N-(5-Nitro-2-thiazolyl)benzamide

Description:
N-(5-Nitro-2-thiazolyl)benzamide is a chemical compound characterized by its thiazole and benzamide functional groups. The presence of a nitro group on the thiazole ring contributes to its potential reactivity and biological activity. This compound typically exhibits a solid state at room temperature and is soluble in organic solvents, which is common for many aromatic compounds. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of antimicrobial or anticancer agents, due to the biological significance of both the thiazole and nitro functionalities. The compound may also display specific spectral characteristics in techniques such as UV-Vis and NMR spectroscopy, aiding in its identification and characterization. Safety data should be consulted, as nitro compounds can pose health risks, including toxicity and environmental hazards. Overall, N-(5-Nitro-2-thiazolyl)benzamide represents a class of compounds with diverse applications in medicinal chemistry and material science.
Formula:C10H7N3O3S
InChI:InChI=1S/C10H7N3O3S/c14-9(7-4-2-1-3-5-7)12-10-11-6-8(17-10)13(15)16/h1-6H,(H,11,12,14)
InChI key:InChIKey=TYUHMMUUMWZPDB-UHFFFAOYSA-N
SMILES:N(C(=O)C1=CC=CC=C1)C=2SC(N(=O)=O)=CN2
Synonyms:
  • 2-Benzamido-5-nitrothiazole
  • Benzamide, N-(5-nitro-2-thiazolyl)-
  • Benzamido-2-nitro-5-thiazole
  • Brn 0023059
  • N-(5-Nitrothiazol-2-yl)benzamide
  • N-(5-nitro-1,3-thiazol-2-yl)benzamide
  • Nsc 87574
  • Thiazole, 2-benzamido-5-nitro-
  • N-(5-Nitro-2-thiazolyl)benzamide
  • N-(5-Nitro-2-thiazolyl)benzamide
  • 4-27-00-04678 (Beilstein Handbook Reference)
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.
  • N-(5-Nitro-thiazol-2-yl)-benzamide
    Biosynth
    + Info

    N-(5-Nitro-thiazol-2-yl)-benzamide

    CAS:
    <p>N-(5-Nitro-thiazol-2-yl)-benzamide is a noncompetitive inhibitor of the enzyme succinate dehydrogenase and is used as an molluscicide. It binds to the active site of the enzyme, which is located in the mitochondrial membrane, and prevents electron transfer from succinate to ubiquinone. This leads to a decrease in production of ATP, which is needed for cell growth and division. N-(5-Nitro-thiazol-2-yl)-benzamide has been shown to inhibit inflammation by inhibiting prostaglandin synthesis in mice. The drug also inhibits neutrophil infiltration into inflamed areas, which may be due to its effect on 5HT2A receptors.</p>
    Formula:C10H7N3O3S
    Purity:Min. 95%
    Molecular weight:249.25 g/mol

    Ref: 3D-PCA39884

    50mg
    344.00€