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5-phenyl-1,3-dithiolo<4,5-b>-1,4-dithiin-2-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

177544-77-3

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177544-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177544-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,5,4 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 177544-77:
(8*1)+(7*7)+(6*7)+(5*5)+(4*4)+(3*4)+(2*7)+(1*7)=173
173 % 10 = 3
So 177544-77-3 is a valid CAS Registry Number.

177544-77-3Relevant academic research and scientific papers

An in depth study of the formation of new tetrathiafulvalene derivatives from 1,8-diketones

Turksoy, Figen,Wallis, John D.,Tunca, Umit,Ozturk, Turan

, p. 8107 - 8116 (2007/10/03)

A detailed study of the reactions of phosphorus pentasulfide and Lawesson's reagent with a series of 4,5-bis(RCOCH 2S)-1,3-dithiole-2-thiones (R=Ph, 4-MeOC6H4, 4-Br C6H4, Me) has been carried out. These reactions lead to fusion of either an unsaturated 1,4-dithiin ring or a thiophene to the dithiole; the former in higher yield, while the latter is a significant product in the reactions with Lawesson's reagent; as well as small amounts of minor products. A mechanistic rationalization of these products is discussed in some detail. The new fused dithioles have been converted to novel series of fused TTF derivatives.

An unusual reaction of Lawesson's reagent with 1,8-diketones: A synthesis of fused 1,4-dithiins and thiophenes

Ozturk, Turan

, p. 2821 - 2824 (2007/10/03)

Reaction of 1,8-diketones 3 with Lawesson's reagent 8 resulted in the formation of five and six-membered rings 5-7, 18, depending on the nature of the substituents. Product 6 is converted in two steps to the unsymmetric 'ET' analogue 20, containing an extra double bond.

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