3090-56-0

Basic information

• Product Name: 2-HYDROXYETHYLVINYLSULPHIDE
• Synonyms: 2-HYDROXYETHYLVINYLSULPHIDE
• CAS NO: 3090-56-0
• Molecular Formula: C₄H₈OS
• Molecular Weight: 104.1707
• Mol File: 3090-56-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 195.3 °C at 760 mmHg
• Flash Point: 95.9 °C
• Appearance: /
• Density: 1.026g/cm³
• Vapor Pressure: 0.899mmHg at 25°C
• Refractive Index: 1.498
• CAS DataBase Reference: 2-HYDROXYETHYLVINYLSULPHIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-HYDROXYETHYLVINYLSULPHIDE(3090-56-0)
• EPA Substance Registry System: 2-HYDROXYETHYLVINYLSULPHIDE(3090-56-0)

Safety Data

• Hazardous Substances Data: 3090-56-0(Hazardous Substances Data)

Usage

General Description

2-Hydroxyethylvinylsulphide is a chemical compound that is classified as a vinyl sulfide derivative. It is also known by its chemical formula C4H8O2S. 2-HYDROXYETHYLVINYLSULPHIDE is used in the synthesis of pharmaceuticals and agrochemicals. It is also used as a crosslinking agent in the production of polymers and as a starting material for the synthesis of other organic compounds. 2-Hydroxyethylvinylsulphide is a colorless liquid with a characteristic odor, and it is important to handle it with caution due to its potential hazards, including skin and eye irritation, and it should be stored in a cool, dry place away from direct sunlight and heat sources.

InChI:InChI=1/C4H8OS/c1-3-6-4(2)5/h3-5H,1H2,2H3

Upstream product

• 81142-02-1 β-chloroethyl vinyl sulfide 
• 505-60-2 bis (2-chloroethyl) sulphide 
• 7647-01-0 hydrogenchloride 
• 4747-16-4 2-(Vinyloxy)ethyl vinyl sulfide 
• 111-48-8 2,2'-thiobis-ethanol 
• 60-24-2 2-hydroxyethanethiol 
• 74-86-2 acetylene 

Downstream Products

• 1158815-73-6 1-benzyl-8,9-dihydro-1H-dibenzo[3,4:7,8]cycloocta[1,2-d][1,2,3]triazole 
• 1427512-50-2 2-((2-methyl-9,10-dihydro-8H-pyrano[2,3-h]quinolin-8-yl)thio)ethanol 
• 1234581-61-3 2-(vinylthio)ethyl 3-[3,5-di(tert-butyl)-4-hydroxyphenyl]propionate 
• 10035-10-6 hydrogen bromide 
• 5244-34-8 2,2'-ethane-1,2-diylbissulfanyl-bis-ethanol 
• 98276-04-1 2-(1-ethylsulfanyl-ethylsulfanyl)-ethanol 
• 57830-41-8 3,6-dithiaoctan-1-ol 

Relevant articles and documents

Metal ferrite nanoparticles: Synthesis, characterization, and studies on decontamination of sulfur mustard

Mg, Ca, Mn, Co, Ni, Cu, Zn, Mn-Zn, and Co-Zn metal ferrite and mixed metal ferrite nanoparticles were synthesized by co-precipitation method and were characterized by using transmission electron microscopy, X-ray diffraction, and nitrogen adsorption techn

Facile hydrolysis-based chemical destruction of the warfare agents VX, GB, and HD by alumina-supported fluoride reagents

(Chemical Equation Presented) A facile solvent-free hydrolysis (chemical destruction) of the warfare agents VX (O-ethyl S-2-(diisopropylamino)ethyl methylphosphonothioate), GB (O-isopropyl methylphosphonofluoridate or sarin), and HD (2,2′-dichloroethyl sulfide or sulfur mustard) upon reaction with various solid-supported fluoride reagents is described. These solid reagents include different alumina-based powders such as KF/Al2O3, AgF/KF/Al2O3, and KF/Al2O3 enriched by so-called coordinatively unsaturated fluoride ions (termed by us as ECUF-KF/Al2O3). When adsorbed on these sorbents, the nerve agent VX quickly hydrolyzed (t1/2 range between 0.1-6.3 h) to the corresponding nontoxic phosphonic acid EMPA as a major product (>90%) and to the relatively toxic desethyl-VX (1/2 range between 2.2-161 h). The reaction rates and the product distribution were found to be strongly dependent on the nature of the fluoride ions in the KF/Al2O 3 matrix and on its water content. All variations of the alumina-supported fluoride reagents studied caused an immediate hydrolysis of the highly toxic GB (t1/2 31P, 13C, and 19F MAS NMR.