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1,5-dimethoxy-2,4-bis-methylsulfanyl-benzene is an organic compound with the molecular formula C10H14O2S2. It features a benzene ring with two methoxy groups (-OCH3) attached to the 1st and 5th carbon atoms, and two methylsulfanyl groups (-SCH3) attached to the 2nd and 4th carbon atoms. 1,5-dimethoxy-2,4-bis-methylsulfanyl-benzene is characterized by its symmetrical structure and the presence of both electron-donating methoxy groups and electron-withdrawing methylsulfanyl groups, which can influence its chemical reactivity and physical properties. It is a colorless liquid with a distinctive odor and is used in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. Due to its complex structure, it is important to handle this chemical with care, following proper safety protocols.

2570-49-2

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2570-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2570-49-2 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 2570-49:
(6*2)+(5*5)+(4*7)+(3*0)+(2*4)+(1*9)=82
82 % 10 = 2
So 2570-49-2 is a valid CAS Registry Number.

2570-49-2Downstream Products

2570-49-2Relevant academic research and scientific papers

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

Mukaiyama, Teruaki,Suzuki, Kaoru

, p. 1 - 4 (1993)

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.

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.

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