10498-56-3

Basic information

• Product Name: 1,4-BIS(DICHLOROPHOSPHINO)BENZENE
• Synonyms: 1,4-BIS(DICHLOROPHOSPHINO)BENZENE
• CAS NO: 10498-56-3
• Molecular Formula: C₆H₄Cl₄P₂
• Molecular Weight: 279.86
• Mol File: 10498-56-3.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,4-BIS(DICHLOROPHOSPHINO)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-BIS(DICHLOROPHOSPHINO)BENZENE(10498-56-3)
• EPA Substance Registry System: 1,4-BIS(DICHLOROPHOSPHINO)BENZENE(10498-56-3)

Safety Data

• Hazardous Substances Data: 10498-56-3(Hazardous Substances Data)

Usage

Uses

Used in Coordination Chemistry:
1,4-Bis(dichlorophosphino)benzene is used as a ligand for forming stable complexes with transition metal ions, which are crucial in catalysis, material science, and pharmaceutical synthesis due to their unique bonding and catalytic properties.
Used in Catalysis:
In the field of catalysis, 1,4-Bis(dichlorophosphino)benzene is used as a component in catalysts that facilitate various chemical reactions, enhancing their efficiency and selectivity.
Used in Material Science:
1,4-Bis(dichlorophosphino)benzene is utilized in the development of new materials with specific properties, such as those required for high-performance electronic devices or advanced coatings.
Used in Pharmaceutical Synthesis:
1,4-BIS(DICHLOROPHOSPHINO)BENZENE is employed as a building block or intermediate in the synthesis of pharmaceuticals, contributing to the creation of new drugs with improved therapeutic properties.
Used in Optoelectronics:
1,4-Bis(dichlorophosphino)benzene is used in the research and development of organic light-emitting diodes (OLEDs) and other optoelectronic devices, capitalizing on its unique electronic and optical properties to enhance device performance.
Used in Research and Development:
In the scientific community, 1,4-Bis(dichlorophosphino)benzene is used as a model compound for studying the properties and reactions of organophosphorus compounds, furthering our understanding of their behavior and potential applications.

Upstream product

• 2425-81-2 phen-1,4-ylenbis(magnesiumbromid) 
• 7270-42-0 1,4-dilithiobenzene 
• 106-37-6 1.4-dibromobenzene 
• 910-42-9 p-phenylenebis(diethylamino)diphosphine 
• 47071-60-3 p-C₆H₄(P(N(CH₃)2)2)2 

Downstream Products

• 95029-23-5 μ-[p-phenylenebis(dichlorophosphane)]-bis(tetracarbonyl)iron 
• 92381-36-7 P,P'-Dimethyl-p-phenylen-diphosphin 
• 324533-99-5 P,P,P',P'-tetrakis(4-triisopropyloxysilylphenyl)p-phenylenediphosphine 
• 183055-33-6 C₆H₄(PClC₆H₂(C₄H₉)3)2 
• 78550-67-1 p-phenylenediphosphine 

Relevant articles and documents

UPE Studies of Conjugation Involving Group 5A Elements. 1. Phenylphosphines

UPE spectra are reported for phenylphosphine, p-phenylenediphosphine, phenyldichlorophosphine, p-phenylenebis(dichlorophosphine), phenylbis(diethylamino)phosphine, and p-phenylenebis(diethylamino)diphosphine.Analysis using PMO theory indicates that the as

Double Clusters Containing Two Ligand-bridged Trinuclear Clusters

Using the patterns for the synthesis of simple RPM3 clusters we obtained M3P-R'-PM3 double clusters.Precursors of the connecting units P-R'-P (R'= p-C6H4 or 4,4'-C6H4-C6H4) were the partially new bifunctional phosphanes X2P-R'-PX2 (X = NEt2, Cl, H).Their