109057-50-3

Basic information

• Product Name: Pentaneselenoic acid Se-phenyl ester
• Synonyms: Pentaneselenoic acid Se-phenyl ester
• CAS NO: 109057-50-3
• Molecular Weight: 241.192
• Mol File: 109057-50-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Pentaneselenoic acid Se-phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Pentaneselenoic acid Se-phenyl ester(109057-50-3)
• EPA Substance Registry System: Pentaneselenoic acid Se-phenyl ester(109057-50-3)

Safety Data

• Hazardous Substances Data: 109057-50-3(Hazardous Substances Data)

Upstream product

• 1666-13-3 diphenyl diselenide 
• 638-29-9 n-valeryl chloride 
• 109057-53-6 (Cyclohex-1-enyl-phenylselanyl-methyl)-trimethyl-silane 
• 109057-45-6 Trimethyl-(1-phenylselanyl-allyl)-silane 
• 14370-82-2 allyl phenyl selenide 
• 84993-35-1 1-Phenylselenenylmethylcyclohexene 

Downstream Products

• 1671-77-8 n-butyl p-tolyl ketone 
• 914220-77-2 1-(4-(tert-butyl)phenyl)pentan-1-one 
• 854659-33-9 1-(2,4-dimethoxyphenyl)pentan-1-one 
• 51770-84-4 1-(2,4-dimethylphenyl)pentan-1-one 
• 66053-97-2 1-(3,4-dimethoxyphenyl) pentan-1-one 
• 56041-76-0 1-(3,4-dimethylphenyl) pentan-1-one 
• 38843-82-2 1-(2,5-dimethoxyphenyl) pentan-1-one 
• 66286-25-7 1-(2,5-dimethylphenyl)pentan-1-one 
• 23351-71-5 1-(2,4,6-trimethylphenyl)-1-pentanone 
• 26672-80-0 1-(4-(dimethylamino)phenyl)pentan-1-one 
• 33489-63-3 1-naphthalen-2-yl-pentan-1-one 
• 2876-60-0 1-(naphthalen-1-yl)pentan-1-one 
• 1671-76-7 p-Methoxyvalerophenon 

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

P -Selective (sp2)-C-H functionalization for an acylation/alkylation reaction using organic photoredox catalysis

p-Selective (sp2)-C-H functionalization of electron rich arenes has been achieved for acylation and alkylation reactions, respectively, with acyl/alkylselenides by organic photoredox catalysis involving an interesting mechanistic pathway.