101327-56-4

Basic information

• Product Name: Se-phenyl(selenothioperoxy)benzoate
• Synonyms: Se-phenyl(selenothioperoxy)benzoate
• CAS NO: 101327-56-4
• Molecular Weight: 293.248
• Mol File: 101327-56-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Se-phenyl(selenothioperoxy)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Se-phenyl(selenothioperoxy)benzoate(101327-56-4)
• EPA Substance Registry System: Se-phenyl(selenothioperoxy)benzoate(101327-56-4)

Safety Data

• Hazardous Substances Data: 101327-56-4(Hazardous Substances Data)

Upstream product

• 1666-13-3 diphenyl diselenide 
• 98-91-9 thiobenzoic acid 
• 5707-04-0 Phenylselenyl chloride 
• 85156-87-2 Benzoylsulfenyl bromide 
• 71098-88-9 N-phenylselanylphthalimide 

Downstream Products

• 117157-00-3 S-3-acetamido-2-(phenylseleno)propyl thiobenzoate 
• 117157-01-4 methyl 4-benzoylthio-3-phenylselenobutyrate 
• 117157-03-6 S-<1-(phenylseleno)cyclopentyl>methyl thiobenzoate 
• 101327-64-4 trans-S-3-(phenylseleno)bicylo<2.2.1>heptan-2-yl thiobenzoate 
• 101327-64-4 exo-cis-S-3-(phenylseleno)bicylo<2.2.1>heptan-2-yl thiobenzoate 
• 101327-59-7 S-3-hydroxy-2-(phenylseleno)propyl thiobenzoate 
• 102614-58-4 S-1-methyl-2-propenyl benzenecarbothioate 
• 7783-06-4 hydrogen sulfide 
• 117157-09-2 (E)-S-dec-2-enyl thiobenzoate 
• 117157-10-5 (Z)-S-dec-2-enyl thiobenzoate 
• 117157-14-9 (E)-3-thiobenzoylallyl acetate 
• 117157-15-0 (Z)-3-thiobenzoylallyl acetate 
• 117157-16-1 (E)-S-3-acetamidoprop-2-enyl thiobenzoate 
• 117157-17-2 (Z)-S-3-acetamidoprop-2-enyl thiobenzoate 

Relevant articles and documents

Acyl Selenyl Sulfides as the Precursors for Reactive Sulfur Species (Hydrogen Sulfide, Polysulfide, and Selenyl Sulfide)

Persulfides are receiving increased attention due to their links to hydrogen sulfide (H2S) and hydrogen polysulfide (H2Sn). Their close analogues selenyl sulfides (RSeSHs), however, have limited literature precedent, and their reactivity and possible role in biology are largely unknown. Here, we devised an acyl selenyl sulfide template to study RSeSH chemistry. Their stability and reactivity toward amines/thiols were studied. These compounds can produce H2S or H2S2 under different conditions, suggesting that RSeSHs are possible intermediates.

A convenient synthesis of S-acyl phenylselenosulfides

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