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19289-17-9

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19289-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19289-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,8 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19289-17:
(7*1)+(6*9)+(5*2)+(4*8)+(3*9)+(2*1)+(1*7)=139
139 % 10 = 9
So 19289-17-9 is a valid CAS Registry Number.

19289-17-9Upstream product

19289-17-9Relevant academic research and scientific papers

Unusual room temperature activation of 1,2-dialkoxyalkanes by niobium and tantalum pentachlorides

Marchetti, Fabio,Pampaloni, Guido,Zacchini, Stefano

, p. 7026 - 7035 (2008)

The outcome of the reactions of MCl5 (M = Nb, 1a; M = Ta, 1b) with 1,2-dialkoxyalkanes [i.e. MeO(CH2)2OMe (dme), EtO(CH2)2OEt, MeOCH2CH(Me)OMe, MeO(CH 2)2OCH2Cl, MeO(CH2) 2O(CH2)2OMe (diglyme)] depends strictly on the stoichiometry. In the 1:1 molar ratio reactions, single C-O bond cleavage occurs, resulting in formation of alkyl chloride and of the complexes MCl 4[O(R)CH(R′)CH2O] [M = Nb, R = Me, R′ = H, 3a; M = Ta, R = Me, R′ = H, 3b; M = Nb, R = Et, R′ = H, 5; M = Nb, R = R′ = Me, 6; M = Nb, R = CH2Cl, R′ = H, 7; M = Nb, R = (CH2)2O(Me)NbCl5, R′ = H, 8], which have been characterized spectroscopically. Moreover, minor amounts of the oxo-bridged adducts MOCl3(dme)MCl5 (M = Nb, 4a; M = Ta, 4b) have been isolated in the reactions involving dme. On the other hand, compounds 1 react with two (or more) equivalents of dme mainly via a multiple C-O bond cleavage process, affording MOCl3(dme) (M = Nb, 2a; M = Ta, 2b), 1,4-dioxane and methyl chloride. The oxychloride compounds MOCl3 (M = Nb, 11a; M = Ta, 11b) have been efficiently obtained by addition of TiCl4 to 2. Compound 2a is reduced in high yield to the Nb(iii) species NbCl 3(dme), 12, upon treatment with SnBu3H. The oxychloride NbOCl3(diglyme), 9, 1,4-dioxane, CH3Cl and the hexachloroniobate salt [MeOCH2CH2OCH2CH 2O(H)Me][NbCl6], 10, have been identified as products of the reaction of 1a with two equivalents of diglyme. The 1 : 2 molar ratio reaction of 1a with MeOCH2CH(Me)OMe gives 2,5-dimethyl-1,4-dioxane. Compound 1a reacts with two equivalents of EtO(CH2)2OEt or MeO(CH2)2OCH2Cl yielding Cl(CH 2)2OCH2CH3 or O(CH 2Cl)2 and diglyme, respectively, but not dioxane, suggesting that fragmentation pathways different from that found for dme are operating. The X-ray molecular structures of 4a, 4b and 10 have been determined.

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