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4,5-Bis-(methylthio)-1,2-dimethoxybenzol is an organic compound characterized by its chemical structure, which includes two methylthio groups attached to the 4 and 5 positions of a benzene ring, and two methoxy groups at the 1 and 2 positions. This molecule is known for its unique properties and potential applications in various fields, such as pharmaceuticals and agrochemicals. It is a colorless to pale yellow solid with a molecular formula of C10H14O2S2 and a molecular weight of 230.35 g/mol. The compound is synthesized through various chemical reactions and is often used as an intermediate in the production of other organic compounds. Due to its specific functional groups, it exhibits interesting chemical reactivity and can be further modified to create a range of derivatives with diverse applications.

2570-47-0

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2570-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2570-47-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,7 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2570-47:
(6*2)+(5*5)+(4*7)+(3*0)+(2*4)+(1*7)=80
80 % 10 = 0
So 2570-47-0 is a valid CAS Registry Number.

2570-47-0Downstream Products

2570-47-0Relevant academic research and scientific papers

Electrophilic substitutions with the electrogenerated sulfenium cation R1-S+

Do, Quang Tho,Elothmani, Driss,Le Guillanton, Georges

, p. 4657 - 4658 (2007/10/03)

The sulfenium cation R1-S+ electrogenerated by oxidation of organic disulfides, reacts with phenols, aromatic ethers and ketones bearing an hydrogen atom in α position, to give alkyl (aryl) sulfanyl compounds.

An Efficient Synthesis of Unsymmetrical Sulfides from Organic Disulfides and Aromatic Compounds

Mukaiyama, Teruaki,Suzuki, Kaoru

, p. 1 - 4 (2007/10/02)

In the presence of an active acidic catalyst generated from SbCl5 and AgSbF6, the sulfenylation reaction of aromatic compounds with organic disulfides smoothly proceeds in refluxing 1,2-dichloroethane to afford the corresponding unsymmetrical sulfides in high yields.

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