5873-93-8

  • Product Name:Diphenyldithioperoxyanhydride
  • MF:C14H10S4
  • Purity:99%
  • Molecular Weight:306.497
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Product Details

Buy cost-effective 99% pure Diphenyldithioperoxyanhydride 5873-93-8 now

  • Molecular Formula:C14H10S4
  • Molecular Weight:306.497
  • Melting Point:94-96°C 
  • Boiling Point:446.8 °C at 760 mmHg 
  • Flash Point:224 °C 
  • PSA:114.78000 
  • Density:1.367 g/cm3 
  • LogP:5.11920 

5873-93-8 Relevant articles

Controlled free radical polymerization in water-borne dispersion using reversible addition-fragmentation chain transfer

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A novel approach to conducting controlle...

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Lu, Jie,Ten Brummelhuis, Niels,Weck, Marcus

, p. 6225 - 6227 (2014)

β-Hairpin formation is one of the fundam...

Ubiquitous Nature of Rate Retardation in Reversible Addition-Fragmentation Chain Transfer Polymerization

Bradford, Kate G. E.,Petit, Leilah M.,Whitfield, Richard,Anastasaki, Athina,Barner-Kowollik, Christopher,Konkolewicz, Dominik

supporting information, p. 17769 - 17777 (2021/11/10)

Reversible addition-fragmentation chain ...

Tert-amyl methyl ether preparation method and light gasoline modification method

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Paragraph 0088, (2018/06/14)

The invention discloses a tert-amyl meth...

Design, synthesis, and phase behaviors of a novel triphenylene-based side chain liquid crystalline diblock copolymer

Ban, Jianfeng,Pan, Lulu,Shi, Bo,Zhang, Hailiang

, p. 13581 - 13588 (2018/08/21)

A novel double Tp-based liquid crystalli...

Synthesis, characterization, and biological interaction of glyconanoparticles with controlled branching

Liau, Walter T.,Bonduelle, Colin,Brochet, Marion,Lecommandoux, Sbastien,Kasko, Andrea M.

, p. 284 - 294 (2015/01/30)

Branched amphiphilic copolymers were syn...

5873-93-8 Process route

carbon disulfide
75-15-0,12122-00-8

carbon disulfide

bromobenzene
108-86-1,52753-63-6

bromobenzene

bis(thiobenzoyl) disulfide
5873-93-8

bis(thiobenzoyl) disulfide

Conditions
Conditions Yield
bromobenzene; With iodine; magnesium; In tetrahydrofuran; at 30 - 75 ℃; for 3h; Inert atmosphere;
carbon disulfide; In tetrahydrofuran; at 0 - 20 ℃; for 3h; Inert atmosphere;
90%
bromobenzene; With magnesium; iodine; In tetrahydrofuran;
carbon disulfide; In tetrahydrofuran;
With dimethyl sulfoxide; iodine; In ethanol; at 20 ℃; for 1h; Further stages.;
82%
bromobenzene; With iodine; magnesium; In tetrahydrofuran;
carbon disulfide; In tetrahydrofuran; at 20 ℃; for 1h;
With p-toluenesulfonyl chloride; In tetrahydrofuran; at 0 - 20 ℃; for 1.5h;
55%
bromobenzene; With iodine; magnesium; In tetrahydrofuran; for 3h;
carbon disulfide; In tetrahydrofuran; for 3h;
With iodine; In water;
carbon disulfide; bromobenzene; With magnesium; In tetrahydrofuran; at 0 ℃; Inert atmosphere;
With water; potassium hexacyanoferrate(III); for 1.5h;
4.88 g
dithiobenzoic acid sodium salt
3682-36-8

dithiobenzoic acid sodium salt

bis(thiobenzoyl) disulfide
5873-93-8

bis(thiobenzoyl) disulfide

Conditions
Conditions Yield
With iodine; In water; at 20 ℃; for 0.25h;
50%
With potassium hexacyanoferrate(III); In water; at 20 ℃; for 1h;
With potassium hexacyanoferrate(III);
With potassium hexacyanoferrate(III); In water; for 1h;
With potassium hexacyanoferrate(III); In water; at 20 ℃; for 1h;
With potassium hexacyanoferrate(III); In water; for 1h;
With potassium hexacyanoferrate (III); for 1h;
With potassium hexacyanoferrate(III); In water; for 1h;

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