2486-04-6

Basic information

• Product Name: 24DINITROBIPHENYL(2,4-DINITROISOMER)
• Synonyms: 24DINITROBIPHENYL(2,4-DINITROISOMER)
• CAS NO: 2486-04-6
• Molecular Formula: C₁₂H₈N₂O₄
• Molecular Weight: 244.20292
• Mol File: 2486-04-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 382°C at 760 mmHg
• Flash Point: 184.1°C
• Appearance: /
• Density: 1.368g/cm³
• Vapor Pressure: 1.07E-05mmHg at 25°C
• Refractive Index: 1.635
• CAS DataBase Reference: 24DINITROBIPHENYL(2,4-DINITROISOMER)(CAS DataBase Reference)
• NIST Chemistry Reference: 24DINITROBIPHENYL(2,4-DINITROISOMER)(2486-04-6)
• EPA Substance Registry System: 24DINITROBIPHENYL(2,4-DINITROISOMER)(2486-04-6)

Safety Data

• Hazardous Substances Data: 2486-04-6(Hazardous Substances Data)

Usage

Family

Dinitrobenzene

Structure

Consists of two benzene rings with nitro groups attached at the 2 and 4 positions

Uses

Widely used in the synthesis of pharmaceuticals, dyes, and pesticides

Classification

Hazardous substance

Toxicity

Considered toxic and a potential environmental hazard

Persistence

It is persistent in the environment

Carcinogenic properties

Considered carcinogenic

Health effects

Can cause skin and eye irritation; prolonged exposure may lead to more serious health effects

Safety precautions

Should be handled with caution; proper safety precautions should be used when handling this chemical

InChI:InChI=1/C12H8N2O4/c15-13(16)10-6-7-11(12(8-10)14(17)18)9-4-2-1-3-5-9/h1-8H

Upstream product

• 934-56-5 trimethyl(phenyl)stannane 
• 78294-96-9 C₄₂H₃₃IN₂O₄P₂Pd 
• 709-49-9 1-iodo-2,4-dinitrobenzene 

Downstream Products

• 188107-70-2 9-methyl-2-nitrocarbazole 
• 14191-22-1 2-nitrocarbazole 

Relevant articles and documents

REACTIONS OF ORGANOMETHALIC COMPOUNDS CATALYZED BY THE COMPLEXES OF TRANSITION METALS. I. COUPLING OF ORGANOTIN COMPOUNDS WITH ARYL HALIDES CATALYZED BY PALLADIUM COMPLEXES

The reactions of organotin compounds RSnMe3 C, C9H7 (indenyl), C13H9 (9-fluorenyl)> with aryl halides ArX , catalyzed by palladium complexes ArPdI(PPh3)2 in dichloroethane under vacuum conditions were investigated.In the reactions of RSnMe3 (where R = Ph, m-CH3C6H4, or PhCC) the RAr compounds are formed with good yields.In the stoichiometric reactions of RSnMe3 (where R = Ph or PhCC) with ArPdI(PPh3)2 (where Ar = Ph, p-NO2C6H4, or 2,4-(NO2)2C6H3> the dimers R2 are formed in addition to RAr, while in the case of the reactions of RSnMe3 (where R = C9H7 or C13H9) only R2 compounds are obtained.The possible mechanisms of the catalytic and stoichiometric reactions are discussed.