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131025-97-3

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131025-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131025-97-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,0,2 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 131025-97:
(8*1)+(7*3)+(6*1)+(5*0)+(4*2)+(3*5)+(2*9)+(1*7)=83
83 % 10 = 3
So 131025-97-3 is a valid CAS Registry Number.

131025-97-3Upstream product

131025-97-3Downstream Products

131025-97-3Relevant academic research and scientific papers

Reactions of cyclopalladated N-nitrosoanilines with SnIV reagents. Crystal structure of the bis cyclopalladated complex cis-Pd2

Albinati, Alberto,Affolter, Samuel,Pregosin, Paul S.

, p. 231 - 254 (2007/10/02)

A series of cyclopalladated N-methyl-N-nitrosoanilines, >2, X = OAc, Cl, Y = 4-OCH3, 4-CH3, 4-NO2, 5-CH3, have been prepared and treated with (i) a variety of reagents to afford mononuclear palladium(II) derivatives, and (ii) R13SnR2 to yield eventually 2-R2 substituted N-methyl-N-nitrosoanalines.The tin(IV) reagents, Me4Sn, Me3SnCCPh, Bun3SnCC(CH2)4CH3, Bun3SnCH=CH2, and Bun3SnCH2CH=CH2 all effectively transfer the R2 group to Pd, but, the mechanisms of the transfer reactions are not necessarily all the same.In some cases the presence of additional ligands, such as PPh3 or (Ph2PCH2)2, are required to suppress side reactions, especially the formation of the bis cyclopalladated complex cis-Pd2, 5.The crystal structure of 5 has been determined by X-ray diffraction methods; relevant bond distances (Angstroem) and bond angles (deg.) are: Pd-N(1) = 2.082(4), Pd-N(3) = 2.078(4); Pd-C(2) = 2.005(4); Pd-C(9) = 1.997(4); N(1)-Pd-N(3) = 99.7(2), N(1)-Pd-C(9) = 168.8(2), N(1)-Pd-C(2) = 79.5(2); C(2)-Pd-C(9) = 102.4(2).It is suggested that the formation of a specific coordination sphere, involving, one cyclometallated ligand, one weakly coordinated ligand, and a monodentate carbon ligand, such as CH3, leads to production of 5.

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