682-91-7

Basic information

• Product Name: Ethylicin
• Synonyms: Ethylicin;S-Ethyl ethanethiosulfonate;ethyl ehtylsulfonothiolate;1-(ethylsulfonylthio)ethane;1-ethylsulfonylsulfanylethane;Ethylicin Solution, 100ppm;S-Ethyl ethanesulfonothioate;ETHYLICIN(WXG01442)
• CAS NO: 682-91-7
• Molecular Formula: C₄H₁₀O₂S₂
• Molecular Weight: 154.25
• Product Categories: FUNGICIDE;NULL
• Mol File: 682-91-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 283.7 °C at 760 mmHg
• Flash Point: 125.4 °C
• Appearance: /
• Density: 1.19 g/cm³
• Vapor Pressure: 0.00533mmHg at 25°C
• Refractive Index: 1.488
• Storage Temp.: Hygroscopic, -20°C Freezer, Under inert atmosphere
• Solubility: Chloroform
• CAS DataBase Reference: Ethylicin(CAS DataBase Reference)
• NIST Chemistry Reference: Ethylicin(682-91-7)
• EPA Substance Registry System: Ethylicin(682-91-7)

Safety Data

• Hazardous Substances Data: 682-91-7(Hazardous Substances Data)

Usage

Uses

Ethylicin can be used for quick rooting powder special for figs.

InChI:InChI=1/C4H10O2S2/c1-3-7-8(5,6)4-2/h3-4H2,1-2H3

Upstream product

• 18542-39-7 ethyl ethanethiosulfinate 
• 1718-44-1 ethanesulfinyl chloride 
• 27482-20-8 cyclohexanone-diethyldithioacetal 
• 7334-52-3 benzaldehyde diethyldithioacetal 
• 76229-69-1 2,2-dimethyl-3,5-dithiaheptane 

Downstream Products

• 34008-91-8 3-(ethylsulfonyl)prop-1-ene 
• 624-89-5 Ethyl methyl sulfide 
• 858835-90-2 1-ethanesulfonyl-1-ethylsulfanyl-acetone 
• 594-45-6 ethanesulfonic acid 
• 81221-65-0 N,N'-bis-(toluene-4-sulfonyl)-ethanesulfinamidyne 
• 3600-24-6 diethyltrisulfane 
• 125208-51-7 C₅H₁₄O₂SSi 
• 4032-81-9 ethyl phenyl disulfide 
• 17640-29-8 ethyl 2-(ethylthio)acetate 
• 837-21-8 ethyl-(2,4-dinitro-phenyl)-sulfone 
• 856060-73-6 ethanesulfonyl-ethylsulfanyl-benzenesulfonyl-methane 
• 856079-24-8 1-ethylsulfanyl-1-(toluene-4-sulfonyl)-acetone 

Relevant articles and documents

Cleavage of S-S bond by nitric oxide (NO) in the presence of oxygen: A disproportionation reaction of two disulfides

Disulfide bond was cleaved by a catalytic amount of nitric oxide in the presence of oxygen, which was confirmed by experiments employing two symmetrical disulfides. The reaction resulted in the formation of unsymmetrical disulfides in nearly 50% yields. The steric hindrance of alkyl disulfide slowed the reaction rate, and an electron-donating group on the aryl disulfide promoted the reaction. The substituent and S-nitrosothiol effects suggested that the reaction was initialized with an oxidative process by NO+.

A Facile Synthesis of Symmetrical Alkanesulfonothioic S-Alkyl Esters (S-Alkyl Alkanethiosulfonates)

-