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4,5-bis(p-nitrobenzylthio)-1,3-dithiole-2-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96133-62-9

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96133-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96133-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,3 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 96133-62:
(7*9)+(6*6)+(5*1)+(4*3)+(3*3)+(2*6)+(1*2)=139
139 % 10 = 9
So 96133-62-9 is a valid CAS Registry Number.

96133-62-9Downstream Products

96133-62-9Relevant academic research and scientific papers

4,5-Bis(benzylthio)-1,3-dithiole-2-thione compounds: Crystal structures of [(p-XC6H4CH2)(p-XC6H 4CH2)dmit: X = Y = OMe; X = Y = NO2; and X = OMe, Y = NO2]

Chohan, Zahid H.,Howie, R. Alan,Wardell, James L.,Wardell, Solange M.S.V.

, p. 1165 - 1172 (2007/10/03)

4,5-Bis(benzylthio)-1,3-dithiole-2-thiones, [(p-XC6H4CH2)(p-XC6H 4CH2)dmit: X = Y = OMe (2); X = OMe, Y = NO2 (3); and X = NO2] (4)] have been prepared from benzyl chlorides and [NEt4]2[Zn(dmit)2]. Isostructural compounds, 2 and 3, crystallize in the triclinic space group P1 (Z = 2) with a = 5.2920(10), b = 10.537(2), c = 18.961(4) A, α = 102.79(3), β = 96.33(3), γ = 98.67(3)° for 2; a = 5.292(8), b = 10.528(12), c = 19.01(2) A, α = 102.74(9), β = 96.26(11), γ = 98.56(11)° for 3. Compound 4 also crystallizes in the space group P1 (Z = 4), with a = 9.296(8), b = 13.993(18), c = 16.186(4) A, α = 106.68(3), β = 89.63(3), γ = 99.38(6)°. Molecular differences between 2 and 3, on one hand, and 4, on the other, arise in the disposition of the aryl rings relative to the dmit group. Short S...S contacts in 2 of 3.320(2) A [S3...S3i (symmetry operation: i: -x + 1, -y + 1, -z)] and in 3 of 3.314(5)A [S3...S3i (symmetry operation: i: -x + 1, -y, -z + 1)] link molecules into pairs. In 4, an S5A...S2B contact of 3.516(5) A links two independent molecules, A and B, into bimolecular units, which are further connected into chains by S2A...S5Bi contacts (symmetry operation: i: x, y, z - 1) at 3.569(5) A. C-H...O hydrogen bonds are also present in 3 and 4.

Donor- und Acceptor-substituierte Tetra(arylthio)tetrathiafulvalene und deren Charge-Transfer-Komplexe mit TCNQ, TCNE und Brom

Mahr, Gerold,Voegtle, Fritz

, p. 2901 - 2909 (2007/10/02)

The syntheses of the new TTF derivatives 1a-g (table 2) and of the thiones 2a-k (table 1) are described.Influences of the substituents R on the dimerization of the thiones 2 and on the charge transfer interactions are noted.The conductivity of electric currency of some of the isolated charge transfer complexes containing TCNQ, TCNE and bromine is described.

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