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547751-72-4

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547751-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 547751-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,7,7,5 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 547751-72:
(8*5)+(7*4)+(6*7)+(5*7)+(4*5)+(3*1)+(2*7)+(1*2)=184
184 % 10 = 4
So 547751-72-4 is a valid CAS Registry Number.

547751-72-4Downstream Products

547751-72-4Relevant articles and documents

Reduction-induced double bond coordination and multiple C-H activation in fully-substituted titanocenes bearing a pendant double bond or an eight-membered hydrocarbyl ansa-chain

Horá?ek, Michal,?těpni?ka, Petr,Kubi?ta, Ji?í,Císa?ová, Ivana,Petrusovaá, Lidmila,Mach, Karel

, p. 154 - 166 (2003)

Reduction of isomeric, fully-substituted titanocene dichlorides having a pendant double bond, the presence of bis(trimethylsilyl)ethyne (btmse) affords different products depending on the alkenyl chain length. Whereas the reduction of 1 yields a compound with intramolecularly η2-coordinated double bond, [Ti(η5-C5Me5) {η2:η5-C5Me4 (CH2CH2CH=CH2)}] (3), compound 2 affords under identical conditions a product with two new Ti-C bonds, [Ti{(η1:η1:η5- C5Me3(CH2)(CH(Me)CH2 CH2)}(η5-C5Me5)] (4). The formation of 3 can be rationalized as a simple intramolecular stabilization of a titanocene intermediate formed by reductive removal of the chloride ligands. The formation of 4 from the respective titanocene, however, requires formally an activation (oxidative addition) of one C-H bond at the methyl group adjacent to the unsaturated chain followed by a hydrogen shift (hydrometallation). Under similar conditions, the complex with asymmetric unsaturated ansa-bridge [TiCl2{η5:η5-C5 Me4CH2CH=CH(CH2)5C 5Me4}] (5) is reduced to a titanocene-η2-alkene complex with the double bond shifted to the central position, ansa-[Ti{η2:η 5:η5-C5Me4 (CH2)3CH=CH(CH2) 3C5Me4}] (7). In the absence of btmse, analogous complex with saturated bridge ansa-[TiCl2{η5:η5 -C5Me4(CH2)8C 5Me4}] (6) undergoes a hydrogen abstraction to give 7 as well albeit in a lower yield. The reduction of 6 in the presence of btmse gives η2-alkyne complex ansa-[Ti{η5:η5-C5Me4 (CH2)8C5Me4} (η2-Me3SiC≡CSiMe3)] (8) which is converted upon thermolysis at 150 °C to a mixture of asym- and sym-isomers of the doubly tucked-in complex ansa-[Ti{(η3:η4-C5Me2 (CH2)2)(CH2)8 (η5-C5Me4)}] (9) in 2:1 ratio; no C-H activation involving methylene groups of the ansa tether was observed. The crystal structures of 4, 7, and 8 have been determined by X-ray crystallography.

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