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(Zn(CF3COO)(C6H5CONHO)(N2C3H4)2) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

896142-02-2

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896142-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 896142-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,6,1,4 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 896142-02:
(8*8)+(7*9)+(6*6)+(5*1)+(4*4)+(3*2)+(2*0)+(1*2)=192
192 % 10 = 2
So 896142-02-2 is a valid CAS Registry Number.

896142-02-2Downstream Products

896142-02-2Relevant academic research and scientific papers

Di-, tri-, and tetranuclear zinc hydroxamate complexes as structural models for the inhibition of zinc hydrolases by hydroxamic acids

Brown, David A.,Fitzpatrick, Noel J.,Muller-Bunz, Helge,Ryan, Aine T.

, p. 4497 - 4507 (2009/06/17)

Attempts to produce Zn analogues of the structural model complexes [M 2(μ-O2CR)2(O2CR) 2(μ-H2O)(tmen)2] (M = Ni, Co, Mn; R = CH3, C(CH3)3, CF3) by the reaction of a series of zinc carboxylates with N,N,N′,N′- tetramethylethylenediamine (tmen), resulted in the mononuclear complexes [Zn(OAc)2(tmen)] (1) and [Zn(crot)2-(tmen)]·0. 5H2O (2) for R = CH3 and (CH)2CH3, respectively, and the dinuclear complexes [Zn2(μ-piv) 2(piv)2(μ-H2O)(tmen)2] (3) and [Zn2(μ-OAcF)2(OAcF) 2(μ-H2O)(tmen)2] (4) for R = C(CH 3)3 and CF3, respectively. In contrast to the analogous imidazole series, i.e., [M2(μ-O2CR) 2(O2CR)2(μ-H2O)(Im)4] (M = Ni, Co, Mn; R = CH3, C(CH3)3, CF 3), zinc carboxylates react with imidazole to give only the mononuclear complexes [Zn(OAc)2(Im)2] (5), [Zn-(crot) 2(Im)2]·H2O (6), [Zn(piv) 2(Im)2]·0.5H2O (7), and [Zn(OAc F)2(Im)2] (8). Reaction of 1, 2, and 3 with either acetohydroxamic acid (AHA) or benzohydroxamic acid (BHA) gives the dinuclear complexes [Zn2(O2CR)3(R′A)- (tmen)], where R′A = acetohydroxamate (AA) (9, 10, 11) or benzohydroxamate (BA) (13, 14, 15). In these complexes, the zinc atoms are bridged by a single hydroxamate and two carboxylates, with a capping tmen ligand on one zinc and a monodentate carboxylate bonded to the second zinc atom. This composition models closely the observed structure of the active site of the p-iodo-D-phenylalanine hydroxamic acid inhibited Aeromonas proteolytica aminopeptidase enzyme. In contrast, 4 reacts with AHA to give [Zn2(OAcF) 3(tmen)2(AA)] (12) with an additional tmen ligand so that both Zn atoms are 6-coordinate, whereas reaction with BHA gives the trinuclear complex [Zn3(OAcF)4(tmen)2(BA) 2] (16). Reactions of 3 and 4 with glutarodihydroxamic acid (GluH2A2) produce the tetranuclear complexes [Zn 4(piv)6(tmen)4(GluA2)] (18) and [Zn4(OAcF)6(tmen)4(GluA 2)] (19).

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