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Propanedithioamide, N,N'-bis(4-methoxyphenyl)-, also known as 4,4'-dimethoxybenzenepropanedithioamide, is an organic compound with the chemical formula C16H18N2O2S2. It is a white crystalline solid that is soluble in organic solvents. Propanedithioamide, N,N'-bis(4-methoxyphenyl)- is characterized by its two 4-methoxyphenyl groups attached to a propane dithioamide backbone, which consists of a propane chain with two硫原子分别连接在两端的氮原子上. It is used as a ligand in coordination chemistry, particularly in the formation of metal complexes, and has potential applications in the synthesis of pharmaceuticals and materials science due to its ability to chelate metal ions.

4887-77-8

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4887-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4887-77-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,8 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4887-77:
(6*4)+(5*8)+(4*8)+(3*7)+(2*7)+(1*7)=138
138 % 10 = 8
So 4887-77-8 is a valid CAS Registry Number.

4887-77-8Relevant academic research and scientific papers

Reactions of malonodithioamides with acetylenedicarboxylic esters

Obydennov,Kosterina,Klimareva,Bakulev,Morzherin

experimental part, p. 1016 - 1018 (2012/02/05)

Reactions of malonothioamides with acetylenedicarboxylates proceed as an addition of the sulfur atom at the triple bond with subsequent intramolecular reaction between the ester group and the nitrogen atom, that leads to substituted thiazolidines. Unsubst

Diversity-orientated synthesis of 3,5-bis(arylamino)pyrazoles

Degorce, Sébastien,Jung, Frédéric H.,Harris, Craig S.,Koza, Patrice,Lecoq, Jonathan,Stevenin, Arnaud

, p. 6719 - 6722 (2012/01/05)

The synthesis of differentially-substituted 3,5-bis(arylamino)pyrazoles has not yet been documented. During our investigation, we managed to develop a novel, entirely combinatorial synthesis of 3,5-bis(arylamino)pyrazoles relying on a simple one-pot two-step operation.

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