10304-75-3

Basic information

• Product Name: 4-chloro(dichloroiodo)benzene
• Synonyms: 4-chloro(dichloroiodo)benzene
• CAS NO: 10304-75-3
• Molecular Weight: 309.361
• Mol File: 10304-75-3.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 4-chloro(dichloroiodo)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro(dichloroiodo)benzene(10304-75-3)
• EPA Substance Registry System: 4-chloro(dichloroiodo)benzene(10304-75-3)

Safety Data

• Hazardous Substances Data: 10304-75-3(Hazardous Substances Data)

Upstream product

• 108-90-7 chlorobenzene 
• 637-87-6 1-Chloro-4-iodobenzene 
• 7647-01-0 hydrogenchloride 
• 75-52-5 nitromethane 
• 7782-50-5 chlorine 
• 7790-99-0 Iodine monochloride 

Downstream Products

• 52207-56-4 1-chloro-4-iodosylbenzene 
• 1246756-23-9 C₁₂H₁₀ClIN₂O 
• 90-98-2 4,4'-Dichlorobenzophenone 
• 34220-01-4 di-(4-chlorophenyl)iodonium chloride 
• 94377-74-9 Bis-<4-chlor-phenyl>-malonsaeure-diaethylester 
• 16825-76-6 1-iodyl-4-chlorobenzene 
• 83-05-6 bis(4'-chlorophenyl)acetic acid 
• 94569-93-4 C₁₄H₁₄ClIO₂ 
• 350-45-8 difluoro(4-chlorophenyl)-λ³-iodane 
• 26018-88-2 bis(4-chlorophenyl)iodonium bromide 

Relevant articles and documents

Willgerodt-Type Dichloro(aryl)-λ 3-Iodanes: A Structural Study

Crystallographic structural analysis of four electronically diverse Willgerodt-type reagents is disclosed together with a solution-phase NMR analysis. These data reveal a plethora of intermolecular non-covalent interactions and confirm the expected T-shape geometry of the reagents. In all cases the I-Cl bonds are orthogonal to the plane of the aryl ring. This study provides important structural insights into this venerable class of dichlorination reagent and has implications for crystal engineering.

Conversion of aryl iodides into aryliodine(III) dichlorides by an oxidative halogenation strategy using 30% aqueous hydrogen peroxide in fluorinated alcohol

Oxidative chlorination with HCl/H2O2 in 1,1,1-trifluoroethanol was used to transform aryl iodides into aryliodine(III) dihalides. In this instance 1,1,1-trifluoroethanol is not only the reaction medium, but is also an activator of hy

A solvent-free synthesis of (dichloroiodo)arenes from iodoarenes

An efficient solid-state oxidation of iodoarenes, ArI, is described using the urea-hydrogen peroxide adduct (UHP), a stable, inexpensive, and easily handled oxidant. The reactions were complete in 15min at 85°C. The melts thus obtained were reacted with e