Difurfuryl sulfide

Available forms:White to brown low melting solid or liquid

pd_proNo:541057-8edb3389-6246-4312-8776-f5a4d17e32df

pd_productuse:

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Detailed introduction

Reliable Quality Difurfuryl sulfide 13678-67-6 Hot Sale with Chinese Manufacturer

  • Molecular Formula:C10H10O2S
  • Molecular Weight:194.254
  • Appearance/Colour:White to brown low melting solid or liquid 
  • Vapor Pressure:0.012mmHg at 25°C 
  • Melting Point:29-34 ºC 
  • Refractive Index:n20/D 1.556(lit.)  
  • Boiling Point:269.4 ºC at 760 mmHg 
  • Flash Point:116.7 ºC 
  • PSA:51.58000 
  • Density:1.195 g/cm3 
  • LogP:3.30600 

Difurfurylsulfide(Cas 13678-67-6) Usage

Preparation

By refluxing a mixture of 2-furyl-methanethiol in ethanolic KOH and furfuryl bromide in ether.

InChI:InChI=1/C10H10O2S/c1-3-9(11-5-1)7-13-8-10-4-2-6-12-10/h1-6H,7-8H2

13678-67-6 Relevant articles

SULFUR EXTRUSION FROM DISULFIDES BY CARBENES

-

Page/Page column 30-31; 36-37, (2021/10/30)

The present invention relates to a metho...

Oxo-rhenium(V) complexes containing heterocyclic ligands as catalysts for the reduction of sulfoxides

Sousa, Sara C. A.,Bernardo, Joana R.,Wolff, Mariusz,Machura, Barbara,Fernandes, Ana C.

, p. 1855 - 1859 (2014/04/03)

This work reports the catalytic activity...

Oxo-Rhenium(V) Complexes Containing Heterocyclic Ligands as Catalysts for the Reduction of Sulfoxides

Sousa, Sara C. A.,Bernardo, Joana R.,Wolff, Mariusz,Machura, Barbara,Fernandes, Ana C.

supporting information, p. 1855 - 1859 (2015/10/05)

This work reports the catalytic activity...

Highly efficient rhenium-catalyzed deoxygenation of sulfoxides without adding any reducing agent

Sousa, Sara C.A.,Bernardo, Joana R.,Rom?o, Carlos C.,Fernandes, Ana C.

experimental part, p. 8194 - 8197 (2012/09/22)

This work reports a novel method for the...

13678-67-6 Process route

2-thiolomethyl-furan
98-02-2,175236-33-6

2-thiolomethyl-furan

difurfuryl sulfide
13678-67-6

difurfuryl sulfide

furfuryl disulfide
4437-20-1

furfuryl disulfide

bis(2-furylmethyl) trisulfide

bis(2-furylmethyl) trisulfide

Conditions
Conditions Yield
With hydrogen sulfide; dimethylglyoxal; In ethanol;
With hydrogen sulfide; dimethylglyoxal; In ethanol; Ambient temperature;
2-thiolomethyl-furan
98-02-2,175236-33-6

2-thiolomethyl-furan

dimethylglyoxal
431-03-8

dimethylglyoxal

difurfuryl sulfide
13678-67-6

difurfuryl sulfide

furfuryl disulfide
4437-20-1

furfuryl disulfide

3-<(2-furylmethyl)dithio>-2-butanone

3-<(2-furylmethyl)dithio>-2-butanone

bis(2-furylmethyl) trisulfide

bis(2-furylmethyl) trisulfide

Conditions
Conditions Yield
With hydrogen sulfide; In ethanol; Further byproducts given;

13678-67-6 Upstream products

  • 98-02-2
    98-02-2

    2-thiolomethyl-furan

  • 431-03-8
    431-03-8

    dimethylglyoxal

  • 28588-74-1
    28588-74-1

    2-methylfuran-3-thiol

  • 1395105-45-9
    1395105-45-9

    difurfuryl sulfoxide

13678-67-6 Downstream products

  • 1383805-16-0
    1383805-16-0

    diphenyl[(furfurylsulfidyl)sulfonium triflate]

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