115072-85-0 Usage
Uses
Used in Coordination Chemistry:
2,4-dichloro-1,3-dicyclohexyl-1,3,2-diazaphosphole is used as a ligand for its ability to coordinate with metal centers, enhancing the stability and reactivity of metal complexes.
Used in Catalysis:
2,4-dichloro-1,3-dicyclohexyl-1,3,2-diazaphosphole serves as a catalyst or a catalyst precursor in various chemical reactions, leveraging its unique coordination properties to facilitate transformations.
Used in Organic Synthesis:
2,4-dichloro-1,3-dicyclohexyl-1,3,2-diazaphosphole is utilized as a reagent or intermediate in organic synthesis, contributing to the formation of complex organic molecules.
Used in Material Science:
It is employed in the development of new materials, such as polymers or coordination polymers, where its phosphole structure and dichloro substitution can impart specific properties to the resulting materials.
Used in Organometallic Chemistry:
2,4-dichloro-1,3-dicyclohexyl-1,3,2-diazaphosphole is used as a component in organometallic compounds, taking advantage of its phosphorus-containing heterocyclic structure to create novel organometallic species with potential applications in catalysis, materials, and beyond.
Check Digit Verification of cas no
The CAS Registry Mumber 115072-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,0,7 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 115072-85:
(8*1)+(7*1)+(6*5)+(5*0)+(4*7)+(3*2)+(2*8)+(1*5)=100
100 % 10 = 0
So 115072-85-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H23Cl2N2P/c15-14-11-17(12-7-3-1-4-8-12)19(16)18(14)13-9-5-2-6-10-13/h11-13H,1-10H2
115072-85-0Relevant articles and documents
The Reaction between Diazadienes and Element Tribromides EBr3 (E = P, B) Revisited: Metal-Free Synthesis of Halogenated N-Heterocyclic Phosphanes and Boranes
Herrmannsd?rfer, Dirk,Kaaz, Manuel,Puntigam, Oliver,Bender, Johannes,Nieger, Martin,Gudat, Dietrich
, p. 4819 - 4828 (2015)
Reactions of selected diazadienes with PBr3 and BBr3 in the presence of a tertiary amine yielding N-heterocyclic phosphanes (NHPs) and N-heterocyclic boranes (NHBs) were studied. It is demonstrated that heterocycle formation occurs e
