73096-40-9

Basic information

• Product Name: 5-(2-Iodophenyl)-1H-tetrazole
• Synonyms: 5-(2-IODOPHENYL)-1H-TETRAZOLE;2-IPT 1H-Tetrazole,5-(2-iodophenyl);5-(2-IODOPHENYL)-1H-TETRAZOLE,99%;5-(2-IODOPHENYL)-1H-TETRAZOLE TRITYL DERIVATIVE IS ALSO AVAILABLE;5-(2-Iodophenyl)-1H-tetrazole
• CAS NO: 73096-40-9
• Molecular Formula: C₇H₅IN₄
• Molecular Weight: 272.05
• Mol File: 73096-40-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 403.187°C at 760 mmHg
• Flash Point: 197.64°C
• Appearance: /
• Density: 2.018g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.706
• CAS DataBase Reference: 5-(2-Iodophenyl)-1H-tetrazole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(2-Iodophenyl)-1H-tetrazole(73096-40-9)
• EPA Substance Registry System: 5-(2-Iodophenyl)-1H-tetrazole(73096-40-9)

Safety Data

• Hazardous Substances Data: 73096-40-9(Hazardous Substances Data)

Usage

General Description

5-(2-Iodophenyl)-1H-tetrazole is a chemical compound belonging to the class of organic compounds known as phenyltetrazoles. This category is characterized by a phenyl ring substituted by a tetrazole ring. The tetrazole ring is a five-membered aromatic ring containing four nitrogen atoms and one carbon atom. Specifically, in the case of 5-(2-Iodophenyl)-1H-tetrazole, the phenyl ring is further substituted at the second position with an iodine atom. It's often used in the field of chemistry as a reagent or a building block in the synthesis of more complex molecules.

InChI:InChI=1/C7H5IN4/c8-6-4-2-1-3-5(6)7-9-11-12-10-7/h1-4H,(H,9,10,11,12)

Upstream product

• 624-84-0 formic acid hydrazide 
• 4387-36-4 2-iodobenzonitrile 

Relevant articles and documents

N-Heterocycle (tetrazole)-stabilized pseudocyclic λ3-iodane: Synthesis and reactivity

An N-heterocycle (tetrazole)-stabilized pseudocyclic λ3-iodane was synthesized and its thermal stability and redox activity were studied. Simultaneous thermogravimetric analysis and differential scanning calorimetry revealed that the polyvalent iodine compound started to degrade at 127 °C and showed a notable exothermic decomposition peak at 147 °C, which was markedly more pronounced than the parent tetrazole with monovalent iodine. The reduction potential was determined by cyclic voltammetry to be ?0.38 V vs AgNO3|Ag in dimethyl sulfoxide at a scan rate of 0.02 V/s. The oxidative power of the polyvalent iodine compound was demonstrated by conducting oxidation of thioanisole to sulfoxide and oxidative dimerization of thiobenzamide to 3,5-diphenyl-1,2,4-thiadiazole.

A Practical Synthesis of 5-Substituted Tetrazoles.

Nitrosation of N-formyl amidrazones 8a-g with sodium nitrite - aqueous hydrochloric acid gives tetrazoles 10a-g in good yields.