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1380397-20-5

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1380397-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1380397-20-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,3,9 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1380397-20:
(9*1)+(8*3)+(7*8)+(6*0)+(5*3)+(4*9)+(3*7)+(2*2)+(1*0)=165
165 % 10 = 5
So 1380397-20-5 is a valid CAS Registry Number.

1380397-20-5Upstream product

1380397-20-5Downstream Products

1380397-20-5Relevant articles and documents

Diverse coordination modes and transformations of allenes at adjacent iridium/osmium centers

MacDougall, Tiffany J.,Ferguson, Michael J.,McDonald, Robert,Cowie, Martin

, p. 4516 - 4528 (2012/07/14)

The methylene-bridged complex, [IrOs(CO)3(μ-CH 2)(dppm)2][BF4] (dppm = μ-Ph 2PCH2PPh2) (2), reacts with allene, resulting in C-C bond formation, to yield an equilibrium mix of two isomers of [IrOs(CO)3(μ-η3:κ1-C(CH 2)3)(dppm)2][BF4] (3/3a), in which the hapticity of the trimethylenemethane ligand with respect to the two metals, as well as the carbonyl ligand arrangement, is different in each isomer. Reaction of 2, as the triflate salt (2-CF3SO3), with methylallene also yields two isomers, [IrOs(CO)3(μ- η3:κ1-C(CHCH3)(CH2) 2)(dppm)2][CF3SO3] (4/4a); however, in this case, the binding mode of the substituted trimethylenemethane moiety is the same in each isomer and differs only in the position of the methyl group on the allylic moiety. The addition of 1,1-dimethylallene to 2-CF 3SO3 results in loss of 4-methyl-1,3-pentadiene and subsequent reaction of the remaining [IrOs(CO)3(dppm) 2]+ species with excess 1,1-dimethylallene to give [IrOs(CO)3(μ-η3:κ1-CH 2CCMe2)(dppm)2][CF3SO3] (5), in which the dimethylallene moiety is κ1-bound to Os through the central carbon and η3-bound to Ir. Both allene and methylallene react with the tetracarbonyl complex, [IrOs(CO)4(dppm) 2][BF4] (6), to generate analogous products, [IrOs(CO)3(μ-η3:κ1-CH 2CCHR)(dppm)2][BF4] (R = H (7), CH3 (8), respectively). Reaction of 6-CF3SO3 with 1,1-dimethylallene yields [IrOs(CO)4(μ-C=C(H)C(CH 3)=CH2)(dppm)2][CF3SO3] (9), the result of activation of the geminal C-H bonds of the unsubstituted end of the allene, and additional activation of a methyl C-H bond. The addition of 1,1-difluoroallene to 6-CF3SO3 yields [IrOs(CO) 4(μ-κ1:κ1-F2C=C= CH2)(dppm)2][CF3SO3] (10), in which this cumulene bridges both metal centers through the central carbon and the CH2 end of the substrate. These reactivities are compared to those of related Ir2, Rh/Ru, Rh/Os, and Ir/Ru complexes.

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