Allyl n-Propyl Sulfide

Available forms:

pd_proNo:493795-3ec01d8e-229f-4801-86ba-0d2ab84a5a8e

pd_productuse:

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Detailed introduction

Manufacturer supply Allyl n-Propyl Sulfide 27817-67-0 with sufficient stock and high standard

  • Molecular Formula:C6H12S
  • Molecular Weight:116.227
  • Vapor Pressure:7.43mmHg at 25°C 
  • Refractive Index:1.462 
  • Boiling Point:141.13 °C at 760 mmHg 
  • Flash Point:30.06 °C 
  • PSA:25.30000 
  • Density:0.85 g/cm3 
  • LogP:2.31560 

ALLYL N-PROPYL SULFIDE(Cas 27817-67-0) Usage

General Description

Allyl N-Propyl Sulfide is a chemical compound that belongs to the family of sulfur-containing organic compounds known as sulfides. It is noted for its strong odor and is a significant part of the unique smells associated with onion and garlic. It is often used as a flavor additive in different types of food products. There is ongoing research into its potential health benefits since preliminary studies suggest that it may have anti-cancer properties. However, it can also cause irritation when it comes into contact with the skin, eyes, or respiratory tract, indicating the need for careful handling.

InChI:InChI=1/C6H12S/c1-3-5-7-6-4-2/h3H,1,4-6H2,2H3

27817-67-0 Relevant articles

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

Deryagina,Korchevin,Russavskaya,Grabel'nykh

, p. 1827 - 1829 (1998)

Allyl halides react with elemental selen...

Antiviral composition derived from allium CEPA and therapeutic use thereof

-

, (2008/06/13)

Novel medicinal extracts derived from Al...

REACTION OF DIALLYL SELENIDE WITH THIOLS

Musorin, G. K.,Amosova, S. V.,Kovaleva, T. V.

, p. 1242 (2007/10/02)

-

Palladium-Catalyzed Synthesis of Allylic and Benzylic Sulifides from the Corresponding Dithiocarbonates

Lu, Xiyan,Ni, Zhijie

, p. 66 - 68 (2007/10/02)

Allylic and benzylic sulfides are prepar...

27817-67-0 Process route

Dithiocarbonic acid O-allyl ester S-propyl ester
58725-93-2

Dithiocarbonic acid O-allyl ester S-propyl ester

allyl-n-propyl suldide
27817-67-0

allyl-n-propyl suldide

Conditions
Conditions Yield
With 1,2-bis-(diphenylphosphino)ethane; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; at 20 ℃; for 10h;
50%
Dithiocarbonic acid S-allyl ester S-propyl ester
109384-46-5

Dithiocarbonic acid S-allyl ester S-propyl ester

allyl-n-propyl suldide
27817-67-0

allyl-n-propyl suldide

Conditions
Conditions Yield
With 1,2-bis-(diphenylphosphino)ethane; tetrakis(triphenylphosphine) palladium(0); In diethyl ether; at 35 ℃; for 8h;
54%

27817-67-0 Upstream products

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    58725-93-2

    Dithiocarbonic acid O-allyl ester S-propyl ester

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    1-thiopropane

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    Diallyl selenide

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