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125495-09-2

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125495-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125495-09-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,4,9 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 125495-09:
(8*1)+(7*2)+(6*5)+(5*4)+(4*9)+(3*5)+(2*0)+(1*9)=132
132 % 10 = 2
So 125495-09-2 is a valid CAS Registry Number.

125495-09-2Downstream Products

125495-09-2Relevant academic research and scientific papers

The chemistry of iron-alkene ions with chlorobenzene

Huang, Yongqing,Freiser, Ben S.

, p. 2052 - 2054 (2008/10/08)

The chemistry of Fe+-alkene ions with chlorobenzene is studied in the gas phase by laser-desorption Fourier transform mass spectrometry. The reaction between Fe+-ethylene and chlorobenzene occurs via initial insertion of Fe+ into the Cl-C bond, followed by ethylene migratory insertion into the Fe+-phenyl bond. Subsequent β-hydrogen abstraction and HCl elimination completes the reaction. In the case of Fe+-propene, a remarkable selectivity governing the migratory insertion step is present, resulting in the formation of Fe+-β-methylstyrene.

Gas-Phase Study of Fe(1+)-Benzyne with Alkanes

Huang, Yongqing,Freiser, Ben S.

, p. 2387 - 2393 (2007/10/02)

The unimolecular chemistry of Fe(1+)-benzyne and its reactivity with small alkanes in the gas phase are studied by Fourier transform mass spectrometry (FTMS).Collision-induced dissociation of Fe(1+)-benzyne yields benzyne loss exclusively.In contrast, photodissociation of Fe(1+)-benzyne yields not only cleavage of benzyne from Fe(1+), but competitive loss of C2H2 and C2H4 as well.The Fe(1+)-benzyne is formed from chlorobenzene by loss of HCl.This dehydrochlorination of chlorobenzene also occurs in secondary reactions up to six times forming products of the typeFe(1+)-polyphenylene.Fe(1+)-benzyne reacts with alkanes larger than methane to form a wide variety of product ions by mechanisms including hydrogenation and methanation of the benzyne ligand.All of the product ions can be explained by mechanisms based on Fe(1+) insertion into either C-C or C-H bonds as the reaction-initiating step, followed by either alkyl or H migration from Fe(1+) onto the benzyne ligand or, alternatively, by the migratory insertion of benzyne into a metal-carbon or metal-hydrogen bond.Photodissociation and ion-molecule reaction studies yield a value for the metal-ligand bond energy of D0(Fe(1+)-benzyne) = 76 +/- 10 kcal/mol.

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