544108
1H-Tetrazole-5-acetic acid
96%
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About This Item
Productos recomendados
Quality Level
assay
96%
mp
180-183 °C (lit.)
functional group
carboxylic acid
SMILES string
OC(=O)Cc1nnn[nH]1
InChI
1S/C3H4N4O2/c8-3(9)1-2-4-6-7-5-2/h1H2,(H,8,9)(H,4,5,6,7)
InChI key
JUNAPQMUUHSYOV-UHFFFAOYSA-N
General description
1H-Tetrazole-5-acetic acid H2tza) can be prepared from ethyl 2-(1H-tetrazol-5-yl)acetate.
Application
1H-Tetrazole-5-acetic acid(H2tza) may be used in the preparation of:
It may also be used as a bifunctional ligand for the synthesis of novel copper(II) and nickel(II) complexes.
- 5-(trinitromethyl)-2H-tetrazole
- N-(furan-2yl methyl)-2-(1H-tetrazol-5-yl)acetamide
- tetrazolium based ionic liquid
It may also be used as a bifunctional ligand for the synthesis of novel copper(II) and nickel(II) complexes.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
Energetic High-Nitrogen Compounds: 5-(Trinitromethyl)-2H-tetrazole and-tetrazolates, Preparation, Characterization, and Conversion into 5-(Dinitromethyl) tetrazoles.
Inorganic Chemistry, 52(12), 7249-7260 (2013)
New Copper (II) and Nickel (II) Complexes with Bifunctional Tetrazolate-5-carboxylate Ligands: Syntheses, Crystal Structures, and Magnetic Properties.
Australian Journal of Chemistry, 62(12), 1622-1630 (2010)
Microwave assisted synthesis of indole and furan derivatives possessing good anti-inflammatory and analgesic activity.
Indian J. Chem. B, 46(11), 1848-1848 (2007)
Synthesis and characterization of silver and gold nanoparticles in ionic liquid.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 73(1), 218-220 (2009)
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