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methyl 3,3-diphenyl-2-(methylthio)dithioacrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59507-59-4

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59507-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59507-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,0 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59507-59:
(7*5)+(6*9)+(5*5)+(4*0)+(3*7)+(2*5)+(1*9)=154
154 % 10 = 4
So 59507-59-4 is a valid CAS Registry Number.

59507-59-4Downstream Products

59507-59-4Relevant articles and documents

PHOTOCHEMICAL REACTIONS OF SOME AROMATIC THIONES WITH BIS(METHYLTHIO)ETHYNE; (4+2)- VERSUS (2+2)-CYCLOADDITION PRODUCTS. SPECTROSCOPIC EVIDENCE FOR THE EQUILIBRIUM THIETE α,β-UNSATURATED DITHIOESTER

Brouwer, A. C.,Bos, H. J. T.

, p. 91 - 95 (2007/10/02)

Irradiation (λ>525 nm) of the aromatic thiones 2 in the presence of bis(methylthio)-ethyne 3 causes two cycloaddition reactions to occur between the photochemically excited thione 2 and the acetylene 3, as concluded from the isolated products.Compounds with structure 6 are believed to be products of a (4+2)-cycloaddition reaction, whereas the formation of the isolated α,β-unsaturated dithio esters 4 is rationalised on the basis of a (2+2)-cycloaddition reaction.The preference for one reaction pathway over the other depends on the thione used is discussed in terms of the structure of the thione 2.Spectroscopic observation of the equilibrium thiete 5 α,β-unsaturated dithio ester 4, in solution provides direct evidence for the (2+2)-photocycloadducts, thietes 5.

Photochemical reactions of some aromatic thiones with bis(methylthio)ethyne; (4+2)- versus (2+2)-cycloaddition products. Spectroscopic evidence for the equilibrium thiete α,β-unsaturated dithioester

Brouwer, A. C.,Bos, H. J. T.

, p. 484 - 488 (2007/10/02)

Irradiation (λ>525 nm) of the aromatic thiones 2 in the presence of bis(methylthio)ethyne 3 causes two cycloaddition reactions to occur between the photochemically excited thione 2 and the acetylene 3, as concluded from the isolated products.Compounds with structure 6 are believed to be products of a (4+2)-cycloaddition reaction, whereas the formation of the isolated α,β-unsaturated dithio esters 4 is rationalised on the basis of a (2+2)-cycloaddition reaction.The preference for one reaction pathway over the other depends on the thione used and is discussed in terms of the structure of the thione 2.Spectroscopic observation of the equilibrium thiete 5 α,β-unsaturated dithio ester 4, in solution provides direct evidence for the (2+2)-photocycloadducts, thietes 5.

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