347744
5-Phenyl-1H-tetrazole
99%
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About This Item
Empirical Formula (Hill Notation):
C7H6N4
CAS Number:
Molecular Weight:
146.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
241-950-8
MDL number:
Assay:
99%
assay
99%
mp
216 °C (dec.) (lit.)
functional group
phenyl
SMILES string
c1ccc(cc1)-c2nnn[nH]2
InChI
1S/C7H6N4/c1-2-4-6(5-3-1)7-8-10-11-9-7/h1-5H,(H,8,9,10,11)
InChI key
MARUHZGHZWCEQU-UHFFFAOYSA-N
General description
Nucleophilic substitution reactions on 1,4-dimethoxybenzene and 1,3,5-trimethoxybenzene by the anions of 5-phenyl-1H-tetrazole has been investigated by paired electrosynthesis.
Application
5-Phenyl-1H-tetrazole may be used as ligand in the solvothermal synthesis of 3D polyoxometalate-based silver coordination polymers. It was used in the synthesis of 5-phenyltetrazolate organolanthanide complexes. It was used to investigate the corrosion inhibition of copper in salt water.
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Min-Xia Liang et al.
Inorganic chemistry, 53(2), 897-902 (2014-01-08)
Four 3D POM-based silver coordination polymers, namely, [Ag17(ptz)11(PW12O40)2]n (1), [Ag17(ptz)11(PMo12O40)2]n (2), [Ag12(ptz)6(CN)2(SiW12O40)]n (3), and [Ag19(ptz)8(H2ptz)(H3ptz)(AgP5W30O110)·7H2O]n (4), have been obtained by solvothermal reaction of AgNO3 and 5-phenyl-1H-tetrazole (Hptz) ligand in the presence of four types of polyoxometalates. Structural analysis shows that
Corrosion inhibition of copper in non-polluted and polluted sea water using 5-phenyl-1-H-tetrazole.
Al Kharafi FM, et al.
International Journal of Electrochemical Science, 7, 3289-3298 (2012)
Nucleophilic aromatic substitution by paired electrosynthesis: Reactions of methoxy arenes with 1H-tetrazoles.
Hu K, et al.
Tetrahedron Letters, 36(39), 7027-7030 (1995)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 347744-100G | 04061833546956 |
| 347744-25G | 04061826761755 |