109057-52-5

Basic information

• Product Name: heptaneselenoic acid Se-phenyl ester
• Synonyms: heptaneselenoic acid Se-phenyl ester
• CAS NO: 109057-52-5
• Molecular Weight: 269.245
• Mol File: 109057-52-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: heptaneselenoic acid Se-phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: heptaneselenoic acid Se-phenyl ester(109057-52-5)
• EPA Substance Registry System: heptaneselenoic acid Se-phenyl ester(109057-52-5)

Safety Data

• Hazardous Substances Data: 109057-52-5(Hazardous Substances Data)

Upstream product

• 109057-45-6 Trimethyl-(1-phenylselanyl-allyl)-silane 
• 141-75-3 butyryl chloride 
• 1666-13-3 diphenyl diselenide 
• 331672-95-8 1H-1,2,3-benzotriazol-1-yl(n-hexyl)methanone 
• 591-51-5 phenyllithium 
• 2528-61-2 Heptanoic acid chloride 
• 84993-35-1 1-Phenylselenenylmethylcyclohexene 
• 14370-82-2 allyl phenyl selenide 
• 5707-04-0 Phenylselenyl chloride 
• 111-14-8 oenanthic acid 
• 109057-53-6 (Cyclohex-1-enyl-phenylselanyl-methyl)-trimethyl-silane 

Downstream Products

• 1056198-20-9 (Z)-8-(phenylselenomethyl)heptadec-8-en-7-one 
• 1056198-21-0 (Z)-1-phenyl-2-(phenylselenomethyl)non-1-en-3-one 
• 1056198-19-6 (Z)-1-cyclohexyl-2-(phenylselenomethyl)non-1-en-3-one 
• 1056198-22-1 (Z)-1-benzyloxy-2-(phenylselenomethyl)non-1-en-3-one 

Relevant articles and documents

Acylation of diselenides and disulfides with N-acylbenzotriazoles promoted by SmI2

The acylation of diselenides or disulfides with N-acylbenzotriazoles mediated by SmI2 has been achieved successfully without the presence of HMPA, and the corresponding selenolesters or thioesters have been prepared in good yields.

Palladium-catalyzed selenoacylation of allenes leading to the regioselective formation of functionalized allyl selenides

(Chemical Equation Presented) Palladium-catalyzed regio- and stereoselective selenoacylation of allenes with selenol esters proceeded to produce functionalized allyl selenides with the acyl moiety at the inner carbon and the SePh group at the terminal car

A regioselective Aluminium Chloride-catalyzed Acylation of Allylic Selenides via α-Silyl Intermediates

The aluminium chloride-catalyzed acylation of α-silylallylic selenides with acid chlorides at -78 deg C produced γ-acylated vinylic selenides regioselectively. α-Silylallylic selenides in some cases underwent shifts of the selenenyl groups by the catalysis with aluminium chloride, affording γ-silylallylic selenides.This regioselective acylation of allylic selenides provides a new route to dihydrojasmone.