di-o-tolyl disulphide

Base Information

  • Chemical Name: di-o-tolyl disulphide
  • CAS No.: 4032-80-8

Factory Export Top Purity di-o-tolyl disulphide 4032-80-8 In Stock

  • Molecular Formula: C14H14 S2
  • Molecular Weight: 246.397
  • Vapor Pressure: 0.000376mmHg at 25°C 
  • Boiling Point: 327.9°Cat760mmHg 
  • Flash Point: 162.9°C 
  • PSA: 50.60000 
  • Density: 1.17g/cm3 
  • LogP: 5.10280 

di-o-tolyl disulphide(Cas 4032-80-8) Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 83, p. 1256, 1961 DOI: 10.1021/ja01466a060

InChI:InChI=1/C14H14S2/c1-11-7-3-5-9-13(11)15-16-14-10-6-4-8-12(14)2/h3-10H,1-2H3

4032-80-8 Relevant articles

Forging C?S(Se) Bonds by Nickel-catalyzed Decarbonylation of Carboxylic Acid and Cleavage of Aryl Dichalcogenides

Zhou, Jing-Ya,Zhu, Yong-Ming

, p. 2452 - 2461 (2021/06/28)

A nickel-catalyzed decarbonylation of ca...

Transformation of arylboronic acids with sodium thiosulfate into organodisulfides catalyzed by a recyclable polyoxometalate-based Cr(iii) catalyst

Chang, Yalin,Li, Huiyi,Tao, Chaofu,Wang, Aiping,Wei, Yongge,Xie, Ya,Yu, Han,Yu, Shunming

supporting information, p. 6059 - 6064 (2021/08/23)

Organo disulfides represent an abundant ...

An unconventional sulfur-to-selenium-to-carbon radical transfer: Chemo-and regioselective cyclization of yne-ynamides

Dutta, Shubham,Prabagar,Vanjari, Rajeshwer,Gandon, Vincent,Sahoo, Akhila K.

, p. 1113 - 1118 (2020/03/11)

An uncommon sulfur → selenium → carbon r...

Palladium-Catalyzed Picolinamide-Directed Benzylic C(sp3)?H Chalcogenation with Diaryl Disulfides and Diphenyl Diselenide

Wang, Kai,Hou, Jiahao,Zhang, Changjun,Cheng, Ke,Bai, Renren,Xie, Yuanyuan

supporting information, p. 2947 - 2952 (2020/06/17)

The first palladium-catalyzed direct ben...

4032-80-8 Process route

toluene
108-88-3,15644-74-3,16713-13-6

toluene

bis(2-methylphenyl)disulfide
4032-80-8

bis(2-methylphenyl)disulfide

phenylmethanethiol
100-53-8

phenylmethanethiol

Conditions
Conditions Yield
With phenoxazine; hydrogen sulfide; Electrochemical reaction;
S-(2-methylphenyl) 2-methylbenzenesulfinothioate
186098-94-2

S-(2-methylphenyl) 2-methylbenzenesulfinothioate

2-methylbenzenesulfinyl chloride
63369-67-5

2-methylbenzenesulfinyl chloride

bis(2-methylphenyl)disulfide
4032-80-8

bis(2-methylphenyl)disulfide

phenyl-<i>o</i>-tolyl disulfide
83878-24-4

phenyl-o -tolyl disulfide

diphenyldisulfane
882-33-7

diphenyldisulfane

Conditions
Conditions Yield
With benzenesulfenyl chloride; In chloroform-d1; at -10 ℃; Yields of byproduct given;
95 % Spectr.

4032-80-8 Upstream products

  • 38045-42-0
    38045-42-0

    S-(2-methylphenyl) 2-methylbenzenesulfonothioate

  • 137-06-4
    137-06-4

    2-thiocresol

  • 133-59-5
    133-59-5

    Toluene-2-sulfonyl chloride

  • 932-31-0
    932-31-0

    ortho-tolylmagnesium bromide

4032-80-8 Downstream products

  • 31171-99-0
    31171-99-0

    Acetyl-o-tolyl-disulfid

  • 101-81-5
    101-81-5

    Diphenylmethane

  • 632-50-8
    632-50-8

    1,1,2,2-tetraphenylethane

  • 42166-14-3
    42166-14-3

    Tetrakis(o-tolylthio)methan

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