65234-93-7

Basic information

• Product Name: 2(3H)-Furanone, dihydro-5-[(phenylseleno)methyl]-
• CAS NO: 65234-93-7
• Molecular Formula: C11H12O2Se
• Molecular Weight: 255.175
• Mol File: 65234-93-7.mol
• Article Data: 29

Chemical Properties

• CAS DataBase Reference: 2(3H)-Furanone, dihydro-5-[(phenylseleno)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(3H)-Furanone, dihydro-5-[(phenylseleno)methyl]-(65234-93-7)
• EPA Substance Registry System: 2(3H)-Furanone, dihydro-5-[(phenylseleno)methyl]-(65234-93-7)

Safety Data

• Hazardous Substances Data: 65234-93-7(Hazardous Substances Data)

Upstream product

• 2179-79-5 phenyl selenocyanate 
• 591-80-0 pent-4-enoic acid 
• 591-50-4 iodobenzene 
• 1666-13-3 diphenyl diselenide 
• 75826-47-0 5-Hydroxy-4-phenylselanyl-pentanoic acid hydrazide 
• 75826-46-9 5-Hydroxy-4-phenylselanyl-pentanoic acid methyl ester 
• 75826-45-8 5-Oxo-4-phenylselanyl-pentanoic acid methyl ester 
• 62030-43-7 pent-4-enoic acid propyl ester 
• 39716-58-0 pent-4-enoyl chloride 
• 923011-86-3 (4S,5R)-2-(3-butenyl)-4-methyl-5-phenyl-4,5-dihydro-1,3-oxazole 
• 34837-55-3 Phenylselenyl bromide 
• 5707-04-0 Phenylselenyl chloride 
• 915127-49-0 N-phenylselenosaccharin 
• 923011-97-6 (1R,2S)-1-phenyl-2-[((2Z)-5-(phenylselenylmethyl)-dihydro-2(3H)-furanylidene)amino]-1-propanol 

Downstream Products

• 693783-96-9 benzyl 4-hydroxy-5-phenylselanylpentanoate 
• 693783-93-6 propyl 4-hydroxy-5-phenylselanylpentanoate 
• 693783-95-8 methyl 4-hydroxy-5-(phenylseleno)pentanoate 
• 19041-15-7 (S)-γ-valerolactone 
• 58917-25-2 (R)-5-methyl-2-oxotetrahydrofuran 
• 1666-13-3 diphenyl diselenide 
• 108-29-2 5-methyl-dihydro-furan-2-one 

Relevant articles and documents

Kinetic Study of the Pyridine-Catalyzed Selenolactonization of 4-Pentenoic Acid

Abstract: The kinetics and mechanism of the pyridine-catalyzed cyclofunctionalization of 4-pentenoic acid by means of PhSeX (X = Cl, Br) have been investigated spectrophotometrically, under pseudo-first order reaction conditions. The influence of the reac

Preparation of selenofunctionalized heterocycles via iodosobenzene-mediated intramolecular selenocyclizations of olefins with diselenides

An intramolecular selenocyclizations of olefins mediated by a commercially available hypervalent iodine(III) reagent, PhIO, was developed. This method provided access to a wide range of selenenylated heterocycles under ambient conditions. The striking advantages of this protocol over all previous methods include mild reaction conditions, easy operation, good yields, high levels of functional group compatibility, large–scale application and suitability for the late-stage functionalization of complex molecules of biological importance.

Electrochemical Difunctionalization of Olefines: Access to Selenomethyl-Substituted Cyclic Ethers or Lactones

A metal- and oxidant-free electrochemical method for preparing selenomethyl-substituted cyclic ethers or lactones via difunctionalization of olefines is presented. A series of selenomethyl-substituted cyclic ethers, particularly 9- and 11- membered, selen