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15081-73-9

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15081-73-9 Usage

Chemical compound

Benzenemethanol, a-[2,2-bis(methylthio)ethenyl]-

Check Digit Verification of cas no

The CAS Registry Mumber 15081-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,8 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15081-73:
(7*1)+(6*5)+(5*0)+(4*8)+(3*1)+(2*7)+(1*3)=89
89 % 10 = 9
So 15081-73-9 is a valid CAS Registry Number.

15081-73-9Relevant articles and documents

Reactions of α-hydroxyketene dithioacetals with Lawesson's reagent: An efficient method for the synthesis of α,β-unsaturated dithioesters

Nair, Satheesh K.,Jose, Ann Maria,Asokan

, p. 1261 - 1264 (2007/10/03)

The α-hydroxyketene dithioacetals 2 and 5, obtained from α-oxoketene dithioacetals by the 1,2-reduction or the 1,2-addition of carbon nucleophiles, on treatment with Lawesson's reagent afforded α,β-unsaturated dithioesters 3 and 6 in good yields. Georg Th

Polarized Ketene Dithioacetals. 28. A New General Highly Stereoselective and Regiospecific Method for Homologation of Ketones to α,β-Unsaturated Esters via α-Oxoketene Dithioacetals

Myrboh, Bekington,Ila, Hiriyakkanavar,Junjappa, Hiriyakkanavar

, p. 5327 - 5332 (2007/10/02)

A new highly stereoselective and regiospecific general method for the conversion of active methylene ketones to α,β-unsaturated O-methyl esters, S-methyl esters, and aldehydes via the corresponding oxoketene dithioacetals has been developed.Thus the carbinols 7a-g obtained by sodium borohydride reduction of the corresponding oxoketene dithioacetals 6a-g, derived from acetophenones and their higher homologues, have been shown to undergo boron trifluoride etherate assisted methanolysis to give the corresponding (E)-methylcinnamates 3a-d and their α-alkyl derivatives 3e-g in high yields.Also the acetals 6h-k derived from alkylmethyl ketones gave the corresponding (E)-methylcrotonates 3h-k.Similarly, the acetals 6l-p derived from alicyclic ketones gave the corresponding cyclic ene esters 3l-p under identical conditions.A few carbinols, 7a-d, were shown to undergo partial hydrolysis in the presence of boron trifluoride etherate/water to give the corresponding S-methyl thiocinnamates 8a-d.The cyclic acetals 6l-n were also similarly converted to the corresponding cyclic S-methylene thio esters 8e-g.The (methylthio)alkenyl ketones 20a-d and 18 after borohydride reduction and acidic hydrolysis gave the corresponding (E)-α,β-unsaturated aldehydes 22a-d and 19.The mechanism governing these transformations has been proposed.

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