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868667-70-3

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868667-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 868667-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,6,6 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 868667-70:
(8*8)+(7*6)+(6*8)+(5*6)+(4*6)+(3*7)+(2*7)+(1*0)=243
243 % 10 = 3
So 868667-70-3 is a valid CAS Registry Number.

868667-70-3Downstream Products

868667-70-3Relevant articles and documents

New palladium(II) and platinum(II) complexes with the model nucleobase 1-methylcytosine: Antitumor activity and interactions with DNA

Ruiz, Jose,Cutillas, Natalia,Vicente, Consuelo,Villa, Maria Dolores,Lopez, Gregorio,Lorenzo, Julia,Aviles, Francesc X.,Moreno, Virtudes,Bautista, Delia

, p. 7365 - 7376 (2008/10/09)

Palladium and platinum complexes with the model nucleobase 1-methylcytosine (1-Mecyt) of the types [Pd(N-N)-(C6F5)(1-Mecyt)]ClO 4 [N-N = bis(3,5-dimethylpyrazol-1-yl)methane (bpzm*), bis(pyrazol-1-yl)methane (bpzm), N,N,N′,N′- tetramethylethylenediamine (tmeda), or 2,2′-bipyridine (bpy)] and [M(dmba)(L′)(1-Mecyt)]CIO4 [dmba = N,C-chelating 2-(dimethylaminomethyl)phenyl; L′ = PPh3 (M = Pd or Pt), DMSO (M = Pt)] have been obtained. Palladium and platinum complexes of the types cis-[M(C6F5)2(1-Mecyt)2] (M = Pd or Pt) and cis-[Pd(L′)(C6F5)(1-Mecyt) 2]ClO4 (L′ = PPh3 or t-BuNC) have also been prepared. The crystal structures of [Pd(bpzm*)(C6F 5)(1-Mecyt)]ClO4, [Pt(dmba)(DMSO)(1-Mecyt)]ClO 4, cis-[Pd(C6F5)2(1-Mecyt) 2], and cis-[Pd(t-BuNC)(C6F5)(1-Mecyt) 2]ClO4 have been established by X-ray diffraction. There is extensive hydrogen bonding (N-H...O, C-H...F or C-H...O) in all the compounds. There are also intermolecular π-π interactions between pyrimidine rings of adjacent chains in [Pd(C6F5) 2(1-Mecyt)2]. DNA adduct formation of the new complexes synthesized was followed by circular dichroism and electrophoretic mobility. Atomic force microscopy images of the modifications caused by the complexes on plasmid DNA pBR322 were also obtained. Values of IC50 were also calculated for the new complexes against the tumor cell line HL-60. At a short incubation time (24 h) almost all new complexes were more active than cisplatin.

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