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((C6H5)3P)2(CH2C(CH3)C(H)CH2)ReH3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81380-34-9

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81380-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81380-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,8 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81380-34:
(7*8)+(6*1)+(5*3)+(4*8)+(3*0)+(2*3)+(1*4)=119
119 % 10 = 9
So 81380-34-9 is a valid CAS Registry Number.

81380-34-9Downstream Products

81380-34-9Relevant articles and documents

REACTION OF (PPh3)2ReH7 WITH DIENES: PREPARATION AND SOME PROPERTIES OF TRIHYDRO η4-DIENE COMPLEXES OF RHENIU

Baudry, Denise,Ephritikhine, Michael,Felkin, Hugh

, p. 363 - 376 (1982)

L2ReH7 (L=PPh3) reacts smoothly with acyclic and cyclic dienes to give crystalline, air-stable, trihydrido-Η4-dienerhenium complexes L2(η4-diene)ReH3.The majority of these complexes are fluxional at room temperature; their NMR spectra suggest that at low temperature (-50 deg C) they are pentagonal bipyramidal, with the two phosphine ligands apical and the remaining ligands equatorial.Except for L2(η4-cyclopentadiene)ReH3, which readily loses dihydrogen to give L2(η5-C5H5)ReH, these diene trihydrides are thermally remarkably stable; L2(η4-cyclohexa-1,3-diene)ReH3 loses dihydrogen at >100 deg C to afford L2(η5-cyclohexadienyl)ReH2 and then L2(η6-C6H6)ReH, and L2(η4-butadiene)ReH3 and L2(η4-cycloocta-1,5-diene)ReH3 are stable in air up to 115 and 130 deg C, respectively.Protonation of the trihydrido-η4-diene complexes affords the corresponding saturated hydrocarbons and/or olefins.Hydrogenation of L2(η4-2,3-dimethylbutadiene)ReH3 regenerates the heptahydride L2ReH7.

Activation des alcanes en catalyse homogene

Aktogu, Nurguen,Baudry, Denise,Cox, David,Ephritikhine, Michel,Felkin, Hugh,et al.

, p. 381 - 385 (2007/10/02)

The first part briefly reports the ionic and radical reactions of satureted hydrocarbons by soluble transition metal complexes.In the second part are described the reactions involving the oxydative addition of a CH bond onto a coordinatively unsaturated organometallic species.The catalytic and selective dehydrogenation of alkanes by rhenium hydrides is presented in the last part.

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