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198490-77-6

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  • Titanium,rel-[(1R)-[1,1'-binaphthalene]-2,2'-diolato(2-)-kO2,kO'2][(1R)-[1,1'-biphenyl]-2,2'-diylbis[(1,2,3,4,5-h)-3,4-dimethyl-2,4-cyclopentadien-1-ylidene]]-

    Cas No: 198490-77-6

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198490-77-6 Usage

General Description

(R)-BIPHENYL-(3,4-DIMETHYL-1-CYCLOPENTADIENYL)-TITANIUM(IV)-(R)-1,1'-BINAPHTHYL-2 is a chemical compound that consists of a titanium atom bonded to a cyclopentadienyl ligand and a binaphthyl ligand. The titanium atom is coordinated to the cyclopentadienyl ligand and the binaphthyl ligand to form a stable coordination complex. (R)-BIPHENYL-(3,4-DIMETHYL-1-CYCLOPENTADIENYL)-TITANIUM(IV)-(R)-1,1'-BINAPHTHYL-2 is commonly used as a catalyst in organic synthesis, particularly in asymmetric catalysis reactions. Its unique structure and coordination properties make it an effective catalyst in promoting various chemical reactions with high selectivity towards the desired chiral products. (R)-BIPHENYL-(3,4-DIMETHYL-1-CYCLOPENTADIENYL)-TITANIUM(IV)-(R)-1,1'-BINAPHTHYL-2 has applications in the pharmaceutical industry, where chiral compounds are of critical importance in drug development and synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 198490-77-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,4,9 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 198490-77:
(8*1)+(7*9)+(6*8)+(5*4)+(4*9)+(3*0)+(2*7)+(1*7)=196
196 % 10 = 6
So 198490-77-6 is a valid CAS Registry Number.

198490-77-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-[2,2'-biphenyldiylbis-(3,4-dimethylcyclopentadienyl)]titanium-(R)-1,1'-bi-2-naphtholate

1.2 Other means of identification

Product number -
Other names (R)-BIPHENYL-(3,4-DIMETHYL-1-CYCLOPENTADIENYL)-TITANIUM(IV)-(R)-1,1'-BINAPHTHYL-2

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:198490-77-6 SDS

198490-77-6Downstream Products

198490-77-6Relevant articles and documents

Asymmetric thermal transformation, a new way to enantiopure biphenyl- bridged titanocene and zirconocene complexes: Efficient catalysts for asymmetric imine hydrogenation

Ringwald, Markus,Stürmer, Rainer,Brintzinger, Hans H.

, p. 1524 - 1527 (2007/10/03)

Enantiopure biphenyl-bridged titanocene and zirconocene complexes were obtained, by an asymmetric thermal transformation of the binaphthol complexes formed from the metallocene racemates and subsequent transformation to the corresponding dichlorides, in practically quantitative yields. Increased rates of this transformation in the presence of O2 gas or TEMPO indicate a radical reaction mechanism. The biphenyl-bridged titanocene enantiomers give rise to an efficient asymmetric catalysis for the hydrogenation of cyclic and noncyclic imines.

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