19708-81-7

Usage

Uses

Used in Organic Synthesis:
Methoxydithioformic acid methyl ester is utilized as a reagent in organic synthesis for various chemical reactions. Its unique properties allow it to act as an intermediate or a building block in the synthesis of different organic compounds.
Used in Polymer Industry:
In the polymer industry, Methoxydithioformic acid methyl ester serves as a stabilizer for certain polymers. Its ability to prevent degradation and maintain the polymer's integrity makes it a valuable additive in the production of specific types of plastics and other polymer-based materials.

InChI:InChI=1/C3H6OS2/c1-4-3(5)6-2/h1-2H3

Upstream product

• 2667-20-1 potassium methylxanthate 
• 67-56-1 methanol 
• 77-78-1 dimethyl sulfate 
• 122118-12-1 N'-phenyl-dithiocarbonohydrazonic acid dimethyl ester 

Downstream Products

• 623-76-7 N,N'-diethylurea 
• 603-54-3 N,N-diphenylurea 
• 20184-98-9 Methyl-3-phenyl-thiocarbazat 
• 60794-34-5 4-benzyl-5-(toluene-4-sulfonylimino)-[1,2,4]dithiazolidin-3-one 
• 19692-07-0 methyl imidothiocarbamate 
• 74-87-3 methylene chloride 
• 87463-12-5 ((Methylthio)carbonyl)(methoxydichloromethyl)disulfane 
• 133958-07-3 3-tert-Butoxy-2-methoxy-thiophene 
• 868-84-8 S,S-dimethyl dithiocarbonate 
• 89264-55-1 bis<(methylthio)carbonyl>disulphane 
• 95271-82-2 bis<(methylthio)carbonyl>trisulphane 
• 95271-83-3 bis<(methylthio)carbonyl>tetrasulphane 
• 95271-84-4 bis<(methylthio)carbonyl>pentasulphane 
• 95271-85-5 bis<(methylthio)carbonyl>hexasulphane 

Relevant academic research and scientific papers

PYRAZOLE DERIVATIVES AS INHIBITORS OF RECEPTOR TYROSYNE KINASES

Compounds of formula (I): and their use in the inhibition of Trk activity are described.

The Synthesis and Reactions of Sterically Constrained Pyrylium and Pyridinium Salts

Efficient syntheses are developed for several pyrylium cations with substitution patterns more sterically demanding than 2,4,6-triphenyl and these are examined as reagents for the conversion of primary amino into a leaving group.The 2-mesityl-4,6-diphenyl derivative did not react smoothly with amines.The 2,6-di-t-butyl-4-phenyl-pyrylium cation gave the corresponding pyridinium derivatives, but they resisted nucleophilic attack. 2-t-Butyl-4,6-diphenylpyridinium cations suffer nucleophilic attack with about the same ease as the 2,4,6-triphenyl analogues.Dihydrobenzopyrylium (6) and tetrahydrodibenzoxanthylium cations (7) gave pyridinium cations which underwent much easier nucleophilic attack: thus they alkylate xanthate anion in ethanol solution and acetate anion in acetic acid.