15325-51-6

Basic information

• Product Name: IsophthalaMidoxiMe, 97%
• Synonyms: IsophthalaMidoxiMe, 97%;Benzene-1,3-diamidoxime
• CAS NO: 15325-51-6
• Molecular Formula: C₈H₁₀N₄O₂
• Molecular Weight: 194.1906
• Mol File: 15325-51-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: IsophthalaMidoxiMe, 97%(CAS DataBase Reference)
• NIST Chemistry Reference: IsophthalaMidoxiMe, 97%(15325-51-6)
• EPA Substance Registry System: IsophthalaMidoxiMe, 97%(15325-51-6)

Safety Data

• Hazard Codes: T
• Statements: 25
• Safety Statements: 45
• RIDADR: UN 2811 6.1 / PGIII
• Hazardous Substances Data: 15325-51-6(Hazardous Substances Data)

Usage

Description

IsophthalaMidoxiMe, 97% is a chemical compound with the molecular formula C8H10N2O2, characterized by its chelating properties and ability to form stable complexes with metal ions, especially copper. It is a white crystalline powder that is moderately soluble in water and has a melting point of around 125-127°C. Known for its relative stability and non-hazardous nature, IsophthalaMidoxiMe, 97% is a versatile compound used in various chemical and industrial processes.

Uses

Used in Pharmaceutical Applications:
IsophthalaMidoxiMe, 97% is used as a chelating agent for its ability to bind with metal ions, which can be crucial in the development of pharmaceuticals that require metal ion management or complexation for enhanced efficacy and stability.
Used in Industrial Applications:
IsophthalaMidoxiMe, 97% is used as a component in the synthesis of coordination polymers and metal-organic frameworks due to its strong affinity for metal ions, facilitating the creation of advanced materials with specific properties for various industrial uses.
Used in Chemical Synthesis:
IsophthalaMidoxiMe, 97% is used as a reagent in the synthesis of other compounds, leveraging its chelating properties to facilitate reactions or to purify products by selectively binding to metal contaminants.

Upstream product

• 626-17-5 benzene-1,3-dicarbonitrile 
• 64-17-5 ethanol 
• 7803-49-8 hydroxylamine 

Downstream Products

• 40067-71-8 5,5'-bis-(chloro-difluoro-methyl)-3,3'-m-phenylene-bis-[1,2,4]oxadiazole 
• 40212-18-8 5,5'-bis-(3-trifluoromethyl-phenyl)-3,3'-m-phenylene-bis-[1,2,4]oxadiazole 
• 40067-69-4 5,5'-bis-(4-trifluoromethyl-phenyl)-3,3'-m-phenylene-bis-[1,2,4]oxadiazole 

Relevant articles and documents

A 1, 2, 4-oxadiazole micromolecule the main body material and its preparation method, application

The invention discloses a 1, 2, 4-oxadiazole micromolecule main body material. The 1, 2, 4-oxadiazole micromolecule main body material contains one or multiple electrophilic 1, 2, 4-oxadiazoles which serve as electron acceptor units, wherein the tail ends of molecules are connected to electron donor units. The invention also discloses a preparation method of the micromolecule main body material. The preparation method is characterized in that a dibromo substituted intermediate, namely a 1, 2, 4-oxadiazole compound is prepared by using bromobenzonitrile as a reaction raw material, and then electron donor units are connected to the dibromo substituted intermediate, namely the 1, 2, 4-oxadiazole compound through Suzuki coupling reaction. The invention also discloses an application of the 1, 2, 4-oxadiazole micromolecule main body material. The 1, 2, 4-oxadiazole micromolecule main body material has relatively good solubility and film-forming property, relatively strong eletrophilicity, relatively low LUMO (Lowest Unoccupied Molecular Orbital) energy level and relatively high electronic mobility.