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Dichloro(p-cymene)tricyclohexylphosphineruthenium(II), min. 97%

Catalog Number
ACM145381233-2
Product Name
Dichloro(p-cymene)tricyclohexylphosphineruthenium(II), min. 97%
Structure
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CAS
145381-23-3
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Synonyms
DICHLORO(P-CYMENE)TRICYCLOHEXYLPHOSPHINERUTHENIUM(II);145381-23-3;MFCD06798308;SC10253;DICHLORO[(1,2,3,4,5,6-H)-1-METHYL-4-(1-METHYLETHYL)BENZENE](TRICYCLOHEXYLPHOSPHINE)RUTHENIUM;
IUPAC Name
dichlororuthenium;1-methyl-4-propan-2-ylbenzene;tricyclohexylphosphane;
Molecular Weight
586.628g/mol
Molecular Formula
C28H47Cl2PRu;
Canonical SMILES
CC1=CC=C(C=C1)C(C)C.C1CCC(CC1)P(C2CCCCC2)C3CCCCC3.Cl[Ru]Cl;
InChI
InChI=1S/C18H33P.C10H14.2ClH.Ru/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-8(2)10-6-4-9(3)5-7-10;;;/h16-18H,1-15H2;4-8H,1-3H3;2*1H;/q;;;;+2/p-2;
InChI Key
SKQOOGIJMPFDJH-UHFFFAOYSA-L;
Complexity
291
Covalently-Bonded Unit Count
3
Exact Mass
586.184g/mol
Heavy Atom Count
32
Monoisotopic Mass
586.184g/mol
Rotatable Bond Count
4
Topological Polar Surface Area
0A^2
Application
Dichloro(p-cymene)tricyclohexylphosphineruthenium(II), min. 97%, is designed to play a pivotal role in advanced polymerization processes. It serves as a Noels metathesis catalyst component when used with (trimethylsilyl)diazomethane, specifically tailored for facilitating ring-opening polymerization reactions. This product is crucial in enabling controlled atom transfer radical polymerization of acrylates, offering precision and efficiency in creating complex polymer structures.
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