Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C2H5N5 |
| Molecular Weight | 99.0946 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NC(N)=NN1
InChI
InChIKey=PKWIYNIDEDLDCJ-UHFFFAOYSA-N
InChI=1S/C2H5N5/c3-1-5-2(4)7-6-1/h(H5,3,4,5,6,7)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis of nickel(II) triazolenaphthalocyanine and related macrocycles. | 2001 Jan 12 |
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| Convenient synthesis of fused heterocyclic 1,3,5-triazines from some N-acyl imidates and heterocyclic amines as anticancer and antioxidant agents. | 2005 Aug |
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| Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005 Jun |
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| Effect of organic additives on the mitigation of volatility of 1-nitro-3,3'-dinitroazetidine (TNAZ): next generation powerful melt cast able high energy material. | 2006 Jun 30 |
|
| Hexaaqua-hexa-kis(μ(2)-3,5-diamino-4H-1,2,4-triazole)trinickel(II) tris-(hexa-fluoridosilicate) icosa-hydrate. | 2008 May 10 |
|
| Oxygen reduction activity of a copper complex of 3,5-diamino-1,2,4-triazole supported on carbon black. | 2009 |
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| Differentiation between [1,2,4]triazolo[1,5-a] pyrimidine and [1,2,4]triazolo[4,3-a]-pyrimidine regioisomers by 1H-15N HMBC experiments. | 2010 Aug |
|
| Diamino-1,2,4-triazole derivatives are selective inhibitors of TYK2 and JAK1 over JAK2 and JAK3. | 2010 Dec 15 |
|
| Metal based biologically active compounds: design, synthesis, and antibacterial/antifungal/cytotoxic properties of triazole-derived Schiff bases and their oxovanadium(IV) complexes. | 2010 Jul |
|
| 3,5-Diamino-1-phenyl-1,2,4-triazolium bromide. | 2010 Jun 16 |
|
| Bis[bis-(3,5-diamino-1H-1,2,4-triazol-4-ium)copper(I)] tris-(hexa-fluoridosilicate). | 2010 Oct 23 |
|
| A carbon-supported copper complex of 3,5-diamino-1,2,4-triazole as a cathode catalyst for alkaline fuel cell applications. | 2010 Sep 8 |
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NCI_THESAURUS |
C272
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1455-77-2
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ACTIVE MOIETY
