3905-96-2

Basic information

• Product Name: 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro-1,1'-biphenyl
• Synonyms: 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro-1,1'-biphenyl;Einecs 223-462-7
• CAS NO: 3905-96-2
• Molecular Formula: C₁₂F₈N₂O₄
• Molecular Weight: 388.1266256
• EINECS: 223-462-7
• Mol File: 3905-96-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 404.3°Cat760mmHg
• Flash Point: 198.3°C
• Appearance: /
• Density: 1.83g/cm³
• CAS DataBase Reference: 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro-1,1'-biphenyl(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro-1,1'-biphenyl(3905-96-2)
• EPA Substance Registry System: 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro-1,1'-biphenyl(3905-96-2)

Safety Data

• Hazardous Substances Data: 3905-96-2(Hazardous Substances Data)

Usage

General Description

2,2',3,3',5,5',6,6'-Octafluoro-4,4'-dinitro-1,1'-biphenyl, also known as octafluoro-1,1'-biphenyl-4,4'-dinitro, is a chemical compound with the molecular formula C12F8N2O4. It is a member of the biphenyl family and is characterized by the presence of eight fluorine atoms and two nitro groups on the biphenyl ring. 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro-1,1'-biphenyl is primarily used as a high-energy density material, and it is also known for its highly energetic and explosive properties. Due to its explosive nature, it is used as a component in certain explosives and propellants. Additionally, it has potential applications in the field of rocket propulsion and as a potential additive to enhance the performance of energetic materials. However, it is important to handle this chemical with extreme care due to its explosive nature.

Upstream product

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Relevant articles and documents

Condensed-ring aryl compound, organic electronic device, and application thereof

The invention provides a condensed-ring aryl compound, an organic electronic device, and an application thereof. The compound has the structure represented as the formula (I) or (II), wherein X1, X2 and Y1 are independently selected from a combination of a connecting bond, N and CR6, the ring A and the ring B are in a conjugated structure, any one of the R1 to R4 and the R6 are independently connected to the ring A the ring B via a single bond or a double bond, and/or the any adjacent two among the R1 to R4 and the R6 form a ring C, being an electron-withdrawing ring, the R5 is selected from aconnection bond, R7-substituted or -non-substituted C6-C30 aryl groups, and R7-substituted or -non-substituted C2-C30 heteroaryl groups, and the R1 to R4, R6 and R7 are electron-withdrawing groups. The compound is free of intramolecular stacking and can prolong service life of the device, wherein the substituent groups are electron-withdrawing groups, and the compound has LUMO energy level of -4.6 to -6.0 eV. The compound can serve as a P-doping material.