30876-65-4

Basic information

• Product Name: 2-phenyl-1-(phenylseleno)ethanone
• Synonyms: 2-phenyl-1-(phenylseleno)ethanone
• CAS NO: 30876-65-4
• Molecular Weight: 275.209
• Mol File: 30876-65-4.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: 2-phenyl-1-(phenylseleno)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-1-(phenylseleno)ethanone(30876-65-4)
• EPA Substance Registry System: 2-phenyl-1-(phenylseleno)ethanone(30876-65-4)

Safety Data

• Hazardous Substances Data: 30876-65-4(Hazardous Substances Data)

Upstream product

• 103-82-2 phenylacetic acid 
• 71098-88-9 N-phenylselanylphthalimide 
• 62762-11-2 β,β-bis(phenylseleno)styrene 
• 6996-92-5 benzeneseleninic acid 
• 937-39-3 2-phenylacetylhydrazine 
• 30665-96-4 2-phenylethynyl phenyl selenide 
• 165278-83-1 (Z)-1-(phenylseleno)-2-phenylethenyl p-toluenesulfonate 
• 41924-21-4 phenyl tributylstannyl selenide 
• 103-80-0 phenylacetyl chloride 
• 134480-05-0 1,1-dichloro-1-phenylseleno methane 
• 1666-13-3 diphenyl diselenide 
• 290820-91-6 bis(phenylselenato)zinc N,N,N',N'-tetramethylethylenediamine 
• 646055-51-8 C₁₃H₁₆O₄ 
• 109-99-9 tetrahydrofuran 

Downstream Products

• 85690-50-2 N-(2-aminobenzyl)-2-phenylacetamide 
• 67630-56-2 N-[2-(benzylamino)ethyl]-2-phenylacetamide 
• 103-82-2 phenylacetic acid 
• 101-97-3 Ethyl 2-phenylethanoate 
• 20343-90-2 bis(phenylseleno)methane 
• 68395-94-8 1-phenyl-3-(phenylseleno)propanone 
• 103-79-7 1-phenyl-acetone 
• 1666-13-3 diphenyl diselenide 
• 20343-91-3 bis(p-tolylseleno)methane 
• 104722-83-0 1-(p-tolylselanyl)propan-2-one 
• 104722-91-0 1-Methyl-4-phenylselanylmethylselanyl-benzene 
• 61759-13-5 1-(phenylselanyl)propan-2-one 
• 104722-82-9 1-phenyl-3-(p-tolylseleno)propanone 
• 5460-60-6 N-phenethyl-2-phenylacetamide 

Relevant articles and documents

Synthesis of selenol esters via the reaction of acyl chlorides with diselenides in the presence of Zn dust catalyzed by CoCl2·6H2O

A practical and efficient approach for the synthesis of selenol and thiol esters is described via the reaction of acyl chlorides with diselenides or disulfides in the presence of Zn dust catalyzed by inexpensive CoCl2·6H2O This proto

Atom efficient preparation of zinc selenates for the synthesis of selenol esters under “On Water” conditions

We describe here an atom efficient procedure to prepare selenol esters in good to excellent yields by reacting [(PhSe)2Zn] or [(PhSe)2Zn]TMEDA with acyl chlorides under “on water” conditions. The method is applicable to a series of aromatic and aliphatic acyl chlorides and tolerates the presence of other functionalities in the starting material.

On water preparation of phenylselenoesters

PhSeZn-halides react under "on water" mild conditions with acid chlorides to provide a high yield route to a variety of aromatic and aliphatic phenylselenoesters.