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173903-47-4 molecular structure
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2-hydroxy-N-(5-nitro-1,3-thiazol-2-yl)benzamide

ChemBase ID: 129935
Molecular Formular: C10H7N3O4S
Molecular Mass: 265.24528
Monoisotopic Mass: 265.01572672
SMILES and InChIs

SMILES:
O=C(Nc1ncc(s1)[N+](=O)[O-])c1ccccc1O
Canonical SMILES:
O=C(c1ccccc1O)Nc1ncc(s1)[N+](=O)[O-]
InChI:
InChI=1S/C10H7N3O4S/c14-7-4-2-1-3-6(7)9(15)12-10-11-5-8(18-10)13(16)17/h1-5,14H,(H,11,12,15)
InChIKey:
FDTZUTSGGSRHQF-UHFFFAOYSA-N

Cite this record

CBID:129935 http://www.chembase.cn/molecule-129935.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
2-hydroxy-N-(5-nitro-1,3-thiazol-2-yl)benzamide
IUPAC Traditional name
tizoxanide
Synonyms
2-Hydroxy-N-(5-nitro-2-thiazolyl)benzamide
NSC 697856
TIZ
Desacetylnitazoxanide
Tizoxanide
CAS Number
173903-47-4
PubChem SID
162224221
PubChem CID
394397
CHEMBL
1545
Chemspider ID
349588
Wikipedia Title
Tizoxanide

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
TRC
T450100 external link Add to cart Please log in.

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 7.8067274  H Acceptors
H Donor LogD (pH = 5.5) 2.2084844 
LogD (pH = 7.4) 2.0683281  Log P 2.2105882 
Molar Refractivity 64.7387 cm3 Polarizability 23.434483 Å3
Polar Surface Area 108.04 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
DMSO expand Show data source
Apperance
Pale Yellow Solid expand Show data source
Melting Point
>240°C (dec) expand Show data source
Storage Condition
-20°C Freezer expand Show data source
MSDS Link
Download expand Show data source
Certificate of Analysis
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DETAILS

DETAILS

Wikipedia Wikipedia TRC TRC
Toronto Research Chemicals - T450100 external link
A metabolite of Nitazoxanide (N490100); a potent inhibitor of hepatitis B virus and hepatitis C virus. Kills Mycobacterium tuberculosis.

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Allen, M., et al.: Hepatology, 27, 1670 (1998)
  • • Blight, K., et al.: Science, 290, 1972 (1998)
  • • Blight, K., et al.: J. Virol., 77, 3181 (1998)
  • • Courcambeck, J., et al.: Antivir Ther., 11, 847 (1998)
  • • Hoffman, P., et al.: Antimicrob. Agents Chemother., 51,
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PATENTS

PATENTS

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INTERNET

INTERNET

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