CAS 14213-11-7

1-(4-Nitrophenyl)-1H-tetrazole

Description:

1-(4-Nitrophenyl)-1H-tetrazole is an organic compound characterized by its tetrazole ring, which is a five-membered heterocyclic structure containing four nitrogen atoms and one carbon atom. The presence of the 4-nitrophenyl group introduces a nitro substituent, which is known for its electron-withdrawing properties, influencing the compound's reactivity and stability. This compound typically exhibits properties such as high thermal stability and potential sensitivity to shock or friction, making it of interest in the field of energetic materials. It is often utilized in research related to explosives and propellants due to its ability to undergo decomposition reactions that release energy. Additionally, 1-(4-Nitrophenyl)-1H-tetrazole may exhibit various solubility characteristics depending on the solvent, and its synthesis often involves reactions that introduce the nitrophenyl group to the tetrazole framework. Overall, this compound is significant in both academic research and practical applications in materials science and chemistry.

Formula: C₇H₅N₅O₂

InChI: InChI=1S/C7H5N5O2/c13-12(14)7-3-1-6(2-4-7)11-5-8-9-10-11/h1-5H

InChI key: InChIKey=NHYHTYJIILODSA-UHFFFAOYSA-N

SMILES: N(=O)(=O)C1=CC=C(C=C1)N2C=NN=N2

Synonyms:

• 1-(4-Nitro-phenyl)-1H-tetrazole
• 1-(4-Nitrophenyl)-1H-1,2,3,4-tetrazole
• 1-(4-Nitrophenyl)-1H-tetraazole
• 1-(4-Nitrophenyl)tetrazole
• 1-(p-Nitrophenyl)-1H-tetrazole
• 1H-Tetrazole, 1- (4-nitrophenyl)-
• 1H-Tetrazole, 1-(p-nitrophenyl)-
• NSC 111925
• 1-(4-Nitrophenyl)-1H-tetrazole
• 1-(4-Nitrophenyl)-1H-tetrazole

1-(4-Nitrophenyl)-1h-1,2,3,4-tetrazole

CAS: 14213-11-7

Purity: 98%

Molecular weight: 191.1499939

Ref: 10-F652329

1-(4-Nitrophenyl)-1H-1,2,3,4-tetrazole

CAS: 14213-11-7

1-(4-Nitrophenyl)-1H-1,2,3,4-tetrazole is a nitroarene that can be used in the synthesis of disubstituted tetrazoles. It reacts with alcohols to form tetrazole compounds and with water to form anhydrides. The high reactivity of 1-(4-Nitrophenyl)-1H-1,2,3,4-tetrazole makes it suitable for use as a reactant in organic synthesis. The regioselectivity of this compound means that it can be used to synthesize only one product from two different starting materials. 1-(4-Nitrophenyl)-1H-1,2,3,4-tetrazole has been shown to react with arylacetonitriles to produce isoxazoles.

Formula: C₇H₅N₅O₂

Purity: Min. 95%

Molecular weight: 191.15 g/mol

Ref: 3D-PAA21311