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Ethanone, 2,2'-(1,2,4-trithiolane-3,5-diylidene)bis[1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19017-95-9

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19017-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19017-95-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,1 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19017-95:
(7*1)+(6*9)+(5*0)+(4*1)+(3*7)+(2*9)+(1*5)=109
109 % 10 = 9
So 19017-95-9 is a valid CAS Registry Number.

19017-95-9Downstream Products

19017-95-9Relevant academic research and scientific papers

REACTION OF 2-BENZOYL- AND 2-NITROETHENE-1,1-DITHIOLATES WITH DIMETHYL ACETYLENEDICARBOXYLATE

Drozd, V. N.,Komarova, E. N.,Dimitriev, L. B.

, p. 1961 - 1965 (2007/10/02)

The reaction of dimethyl acetylenedicarboxylate with 2-benzoyl- and 2-nitroethene-1,1-dithiolates leads to 2-alkylidene-4,5-dimethoxycarbonyl-1,3-dithiolanes (in the form of an equilibrium mixture of the trans and cis isomers).A series of side products are also formed under the reaction conditions. 2,3,4,5-Tetramethoxycarbonylthiophene and 3,5-di(benzoylmethylene)-1,2,4-trithiolane were identified among them.

1,1',2,2'-Tetrathiafulvalenes, II. - Thienothiophenes from 1,2-Dithiole Compounds; 3H-1,2-Dithiol-3-ylidenes (1,2-Dithiole-3-carbenes) as Supposed Intermediates

Behringer, Hans,Meinetsberger, Eike

, p. 1729 - 1750 (2007/10/02)

3,3'-Bi(3H-1,2-dithiolylidenes) (1,1',2,2'-Tetrathiafulvalenes) 5 are not obtainable with the following reactions which, however, have proved to be a good approach to the corresponding 1,3-isomers 3: 1) Deprotonation of 1,2-dithiolylium cations 4, 2) pyrolysis of alkali derivatives from 1,2-dithiol-2-one tosylhydrazones 26 (Bamford-Stevens reaction), or 3) partial desulfuration of 1,2-dithiole-3-thiones 6 by means of trivalent phosphorus compounds.These reactions with the 1,2-isomers always yield thienothiophenes 8 accompanied by the related 1,2-dithiole-3-thiones 6 (1,2-trithiones) and in the case of 26 also by azines 27.Partial desulfuration of 1,2-trithiones 6 by copper bronze again yields the corresponding thienothiophenes 8 instead of 5.Thermal decomposition of the 1,2-dithiolylium iodide 34 or 34' yields the thienothiophene 8a together with the 1,2-trithione 6a.Surprisingly, the P4S10-sulfuration of "desaurines" 37 gives thienothiophenes again and also 1,2-dithiole-3-thiones 6. - 1-Morpholinocyclohexene (18) reacts with the 1,2-dithiolylium cation 4a (X = ClO4) to give a formal 1:1 adduct from the carbene 9a and the enamine for which the structure 19 is proposed.

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