662623
Bis[rhodium(α,α,α′,α′-tetramethyl-1,3-benzenedipropionic acid)]
95%
Synonym(s):
Rh2(esp)2
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About This Item
Empirical Formula (Hill Notation):
C32H40O8Rh2
CAS Number:
Molecular Weight:
758.47
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
95%
form
solid
reaction suitability
core: rhodium
reagent type: catalyst
reaction type: C-H Activation
mp
>300 °C
SMILES string
[Rh][Rh].CC(C)(Cc1cccc(CC(C)(C)C(O)=O)c1)C(O)=O.CC(C)(Cc2cccc(CC(C)(C)C(O)=O)c2)C(O)=O
InChI
1S/2C16H22O4.2Rh/c2*1-15(2,13(17)18)9-11-6-5-7-12(8-11)10-16(3,4)14(19)20;;/h2*5-8H,9-10H2,1-4H3,(H,17,18)(H,19,20);;
InChI key
OBMUTUNJWNQIAJ-UHFFFAOYSA-N
General description
Bis[rhodium(α,α,α′,α′-tetramethyl-1,3-benzenedipropionicacid)] has been identified as efficient C-H activation catalyst.
Application
Bis[rhodium(α,α,α′,α′-tetramethyl-1,3-benzenedipropionicacid)] is used as a catalyst for oxidative C−H amination of urea and guanidinederived substrates to yield corresponding heterocyclic products.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Kristin Williams Fiori et al.
Journal of the American Chemical Society, 129(3), 562-568 (2007-01-18)
Reaction methodology for intermolecular C-H amination of benzylic and 3 degrees C-H bonds is described. This process uses the starting alkane as the limiting reagent, gives optically pure tetrasubstituted amines through stereospecific insertion into enantiomeric 3 degrees centers, displays high
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