5296-62-8

Basic information

• Product Name: ALLYL ETHYL SULFIDE
• Synonyms: ALLYL ETHYL SULFIDE;ALLYL ETHYL SULPHIDE;4-thia-1-hexene;3-Ethylthio-1-propene;Ethyl(2-propenyl) sulfide;Ethylallyl sulfide;3-(ethylthio)prop-1-ene;3-ethylsulfanylprop-1-ene
• CAS NO: 5296-62-8
• Molecular Formula: C₅H₁₀S
• Molecular Weight: 102.2
• Product Categories: monomer
• Mol File: 5296-62-8.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 115-116°C
• Flash Point: 115-116°C
• Appearance: /
• Density: 0,878 g/cm3
• Vapor Pressure: 22.2mmHg at 25°C
• Refractive Index: 1.4680
• BRN: 1736876
• CAS DataBase Reference: ALLYL ETHYL SULFIDE(CAS DataBase Reference)
• NIST Chemistry Reference: ALLYL ETHYL SULFIDE(5296-62-8)
• EPA Substance Registry System: ALLYL ETHYL SULFIDE(5296-62-8)

Safety Data

• Statements: 11-36/37/38
• Safety Statements: 16-23-26-36
• RIDADR: 1993
• HazardClass: 3
• PackingGroup: III
• Hazardous Substances Data: 5296-62-8(Hazardous Substances Data)

Usage

General Description

Allyl ethyl sulfide is a chemical compound commonly found in garlic and other members of the Allium family, which gives them their characteristic odor and flavor. It is a colorless liquid with a strong, pungent odor and is commonly used as a flavoring agent in food. Allyl ethyl sulfide is also known for its potential health benefits, including its antimicrobial and anticancer properties. It is considered safe for consumption in small amounts, but may cause irritation or allergic reactions in some individuals. In high concentrations, it can be toxic and should be handled and used with caution.

InChI:InChI=1/C5H10S/c1-3-5-6-4-2/h3H,1,4-5H2,2H3

Upstream product

• 106-95-6 allyl bromide 
• 811-51-8 sodium thioethylate 
• 40069-87-2 (Z)-ethyl prop-1-enyl sulfide 
• 61865-98-3 (E)-ethyl prop-1-enyl sulfide 
• 107-05-1 3-chloroprop-1-ene 
• 75-08-1 ethanethiol 
• 463-49-0 1,2-propanediene 
• 33458-36-5 ethanethiol-D₁ 
• 24857-04-3 triethylallyltin 
• 127699-25-6 Diallyl selenide 
• 110-81-6 Diethyl disulfide 
• 74-96-4 ethyl bromide 
• 870-23-5 prop-2-ene-1-thiol 

Downstream Products

• 34008-91-8 3-(ethylsulfonyl)prop-1-ene 
• 53097-28-2 (E/Z)-1-(phenylthio)buta-1,3-diene 
• 65597-71-9 (1-Ethylsulfanyl-but-3-enylsulfanyl)-benzene 
• 34757-40-9 ethyl 2-propenyl sulfoxide 
• 110815-12-8 15-(tert-Butyl-diphenyl-silanyloxy)-17-ethylsulfanyl-16-hydroxy-nonadec-18-enoic acid methyl ester 
• 218618-79-2 (2-Allyl-phenoxy)-trimethyl-silan 
• 187737-37-7 propene 
• 6851-93-0 thioacetaldehyde 
• 77896-89-0 R*,S*-3-ethylthio-4-phenyl-1-butenol-4 
• 83877-52-5 (E)-4-Ethylsulfanyl-1-phenyl-but-3-en-1-ol 
• 94633-60-0 4-tert-Butyl-1-(1-ethylsulfanyl-allyl)-cyclohexanol 
• 83877-53-6 4-tert-Butyl-1-((E)-3-ethylsulfanyl-allyl)-cyclohexanol 
• 83877-54-7 (E)-5-Ethylsulfanyl-2-phenyl-pent-4-en-2-ol 

Relevant articles and documents

Ruthenium-catalyzed decarboxylative C-S cross-coupling of carbonothioate: synthesis of allyl(aryl)sulfide

A novel ruthenium-catalyzed decarboxylative cross-coupling of carbonothioate is disclosed. This method provides straightforward access to the corresponding allyl(aryl)sulfide derivatives in generally good to excellent yields under mild conditions and feat

A mechanism of the hydrogenation of the double bond in the synthesis of allyl chalcogenides in the hydrazine hydrate - Potassium hydroxide system

Allyl halides react with elemental selenium in the N2H4 · H2O-KOH system to give diallyl chalcogenides and allyl propyl chalcogenides. The latter form only in the presence of oxygen when unsaturated intermediates CH2=CHCH2YK (Y = S and Se), which are soluble in hydrazine hydrate, are hydrogenated with diimide.

REACTION OF DIALLYL SELENIDE WITH THIOLS

-