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24807-55-4

24807-55-4 | 1H-1,2,4-Triazole, 5-nitro-

CAS No: 24807-55-4 Catalog No: AG002PHU MDL No:MFCD00009749

Product Description

Catalog Number:
AG002PHU
Chemical Name:
1H-1,2,4-Triazole, 5-nitro-
CAS Number:
24807-55-4
Molecular Formula:
C2H2N4O2
Molecular Weight:
114.0629
MDL Number:
MFCD00009749
IUPAC Name:
5-nitro-1H-1,2,4-triazole
InChI:
InChI=1S/C2H2N4O2/c7-6(8)2-3-1-4-5-2/h1H,(H,3,4,5)
InChI Key:
KUEFXPHXHHANKS-UHFFFAOYSA-N
SMILES:
[O-][N+](=O)c1ncn[nH]1
EC Number:
246-468-1
NSC Number:
133107

Properties

Complexity:
98.7  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
114.018g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
114.064g/mol
Monoisotopic Mass:
114.018g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
87.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.1  

Literature

Title Journal
Synthesis, radiolabeling and biological evaluation of propylene amine oxime complexes containing nitrotriazoles as hypoxia markers. Molecules (Basel, Switzerland) 20120604
Coordination of mercury(II) to gold nanoparticle associated nitrotriazole towards sensitive colorimetric detection of mercuric ion with a tunable dynamic range. The Analyst 20110421
Michael-type addition of azoles of broad-scale acidity to methyl acrylate. Beilstein journal of organic chemistry 20110101
3-Nitro-1H-1,2,4-triazole. Acta crystallographica. Section E, Structure reports online 20110101
Pre-clinical evaluation of a 3-nitro-1,2,4-triazole analogue of [18F]FMISO as hypoxia-selective tracer for PET. Nuclear medicine and biology 20100701
A simple approach for predicting impact sensitivity of polynitroheteroarenes. Journal of hazardous materials 20090730
Ruthenium(III) maltolato-nitroimidazole complexes: synthesis and biological activity. Journal of inorganic biochemistry 20061201
The first nitro-substituted heteroscorpionate ligand. Inorganic chemistry 20050221
Synthesis and anti-tuberculosis activity of N-aryl-C-nitroazoles. European journal of medicinal chemistry 20041001

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