915127-49-0

Basic information

• Product Name: 1,2-Benzisothiazol-3(2H)-one, 2-(phenylseleno)-, 1,1-dioxide
• CAS NO: 915127-49-0
• Molecular Formula: C13H9NO3SSe
• Molecular Weight: 338.245
• Mol File: 915127-49-0.mol

Chemical Properties

• CAS DataBase Reference: 1,2-Benzisothiazol-3(2H)-one, 2-(phenylseleno)-, 1,1-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Benzisothiazol-3(2H)-one, 2-(phenylseleno)-, 1,1-dioxide(915127-49-0)
• EPA Substance Registry System: 1,2-Benzisothiazol-3(2H)-one, 2-(phenylseleno)-, 1,1-dioxide(915127-49-0)

Safety Data

• Hazardous Substances Data: 915127-49-0(Hazardous Substances Data)

Upstream product

• 5707-04-0 Phenylselenyl chloride 
• 2673-17-8 1,2-benzisothiazol-3(2H)-one-1,1-dioxide, silver salt 
• 34837-55-3 Phenylselenyl bromide 
• 108-86-1 bromobenzene 
• 1666-13-3 diphenyl diselenide 

Downstream Products

• 51558-95-3 1-phenyl-2-(phenylselanyl)ethanol 
• 116316-12-2 1-azido-1-phenyl-2-(phenylseleno)ethane 
• 63603-28-1 1-methoxy-1-phenyl-2-phenylselenoethane 
• 73090-30-9 trans-1-phenylseleno-2-methoxycyclooctane 
• 116117-92-1 1,2-diphenyl-1-methoxy-2-phenylselenenyl ethane 
• 63603-31-6 methyl 1-phenylselenenyl-2-octyl ether 
• 65539-72-2 2-(phenylselanylmethyl)oxolane 
• 61759-16-8 (2-Phenylseleno)heptanal 
• 65234-93-7 5-phenylselanylmethyl-dihydro-furan-2-one 
• 80448-01-7 p-methoxyphenyl phenyl selenide 
• 80448-00-6 (2-methoxyphenyl)(phenyl)selane 
• 80461-61-6 4-(N,N-dimethylamino)phenyl phenyl selenide 
• 144027-22-5 2-(phenylselanyl)-2,3-dihydro-1H-inden-1-one 

Relevant articles and documents

N-Phenylselenosaccharin (NPSSac): a new electrophilic selenium-containing reagent

A new reagent N-phenylselenosaccharin (NPSSac) was simply prepared and used as a source of the electrophilic phenylselenyl group. This relatively stable new compound was able to react with a series of electron rich organic molecules like alkenes in the pr

Synthesis method of selenium-containing isochroman compound

The invention discloses a synthesis method of a selenium-containing isochroman compound. The synthesis method comprises the following steps: under the protection of nitrogen, adding N-phenylseleno saccharin (NPSSac) into a reactor, then adding dichloromethane to completely dissolve the N-phenylseleno saccharin, adding a 1-[(cinnamoxy) methyl]-3, 4, 5-trimethoxy benzene compound and boron trifluoride diethyl etherate after the N-phenylseleno saccharin is completely dissolved, stirring at 20-60 DEG C for 2-6 hours until the reaction is complete, and after the reaction is finished, quenching, extracting, combining organic phases, drying, concentrating, separating and purifying to obtain the selenium-containing isochroman compound. The synthesis method disclosed by the invention is relatively easy to operate, mild in reaction condition, relatively high in yield, environment-friendly and suitable for large-scale industrial production.