Bis(2-methyl-3-furyl)disulfide

Available forms:clear yellow to amber or orange liquid

pd_proNo:541053-875cae2c-ec4a-4377-9a28-340daa71d37d

pd_productuse:

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Detailed introduction

Perfect Factory Offer Excellent quality Bis(2-methyl-3-furyl)disulfide 28588-75-2 with Safe Shipping

  • Molecular Formula:C10H10O2S2
  • Molecular Weight:226.32
  • Appearance/Colour:clear yellow to amber or orange liquid 
  • Vapor Pressure:0.0118mmHg at 25°C 
  • Refractive Index:1.572-1.583  
  • Boiling Point:269.7 °C at 760 mmHg 
  • Flash Point:116.9 °C 
  • PSA:76.88000 
  • Density:1.29 g/cm3 
  • LogP:4.28880 

Bis(2-methyl-3-furyl)disulfide(Cas 28588-75-2) Usage

InChI:InChI=1/C10H10O2S2/c1-7-9(3-5-11-7)13-14-10-4-6-12-8(10)2/h3-6H,1-2H3

28588-75-2 Relevant articles

Sulfur-Containing Furans in Commercial Meat Flavorings

Ruther, Joachim,Baltes, Werner

, p. 2254 - 2259 (1994)

The volatiles of eight commercially avai...

Method for synthesizing bis(2-methyl-3-furyl) disulfide

-

Paragraph 0057; 0078-0081; 0109-0115; 0136-0139; 0160-0162, (2017/07/19)

The invention relates to a method for sy...

An efficient and convenient method for the preparation of disulfides from thiols using oxygen as oxidant catalyzed by tert-butyl nitrite

Yi, Shan-Li,Li, Mei-Chao,Hu, Xin-Quan,Mo, Wei-Min,Shen, Zhen-Lu

, p. 1505 - 1508 (2016/09/23)

An efficient and convenient tert-butyl n...

Aerobic oxidation of thiols to disulfides under ball-milling in the absence of any catalyst, solvent, or base

Chatterjee, Tanmay,Ranu, Brindaban C.

, p. 10680 - 10686 (2013/09/02)

An efficient aerobic chemoselective oxid...

Novel conversion of thiols into disulfides, via S-nitrosothiol intermediates using trichloronitromethane

Demir, Ayhan S.,Igdir, A. Cigdem,Mahasneh, Ali S.

, p. 12399 - 12404 (2007/10/03)

An efficient oxidative coupling of thiol...

28588-75-2 Process route

2-methylfuran-3-thiol
28588-74-1

2-methylfuran-3-thiol

2-methyl-3-(2-(2-methylfuran-3-yl)disulfanyl)furan
28588-75-2

2-methyl-3-(2-(2-methylfuran-3-yl)disulfanyl)furan

Conditions
Conditions Yield
With aluminum oxide; In neat (no solvent); for 0.416667h; chemoselective reaction; Milling;
97%
With chloropicrin; sodium ethanolate; In acetonitrile; at 20 ℃; for 3h;
94%
With tert.-butylnitrite; oxygen; In 1,2-dichloro-ethane; at 50 ℃; for 4h; under 760.051 Torr; Sealed tube; Green chemistry;
93%
With copper(II) sulfate; In diethyl ether; for 0.5h;
With 2-thiolomethyl-furan; In ethanol;
2-methylfur-3-yl thiocyanate
149428-24-0

2-methylfur-3-yl thiocyanate

2-methyl-3-(2-(2-methylfuran-3-yl)disulfanyl)furan
28588-75-2

2-methyl-3-(2-(2-methylfuran-3-yl)disulfanyl)furan

Conditions
Conditions Yield
With sodium hydroxide; In water; Ambient temperature;
84%
With sodium hydroxide; In water; at 25 - 30 ℃; for 24h; Temperature; Large scale;
22.62 kg

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    2-methylfuran-3-thiol

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