1620673-69-9

Basic information

• Product Name: 4-(4-(phenylselanyl)phenyl)morpholine
• Synonyms: 4-(4-(phenylselanyl)phenyl)morpholine
• CAS NO: 1620673-69-9
• Molecular Weight: 318.277
• Mol File: 1620673-69-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-(4-(phenylselanyl)phenyl)morpholine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-(phenylselanyl)phenyl)morpholine(1620673-69-9)
• EPA Substance Registry System: 4-(4-(phenylselanyl)phenyl)morpholine(1620673-69-9)

Safety Data

• Hazardous Substances Data: 1620673-69-9(Hazardous Substances Data)

Upstream product

• 5707-04-0 Phenylselenyl chloride 
• 92-53-5 4-Phenylmorpholine 
• 1666-13-3 diphenyl diselenide 

Relevant articles and documents

DMSO/iodine-catalyzed oxidative C-Se/C-S bond formation: A regioselective synthesis of unsymmetrical chalcogenides with nitrogen- or oxygen-containing arenes

A convenient metal-free and solvent-free iodine-catalyzed regioselective greener protocol to access different types of unsymmetrical chalcogenides with nitrogen- or oxygen-containing arenes through oxidative C-Se/C-S formation via direct C(sp2)-H bond activation was developed. The products were obtained in good to excellent yields using [O or N]-containing arenes, half equiv. of various odorless diorganyl dichalcogenides (S/Se), iodine (20 mol%) as the catalyst and 3 equiv. of DMSO as the oxidant, applying MW irradiation for 10 min.

Rose Bengal catalysed photo-induced selenylation of indoles, imidazoles and arenes: A metal free approach

In this report, the highly efficient Rose Bengal-catalysed C(sp2)-H selenylation of indoles, imidazoles and arenes was achieved using a half molar equiv. of diorganoyl diselenides. This metal-free, photo-induced protocol resulted in selenylated

Metal and base-free synthesis of arylselanyl anilines using glycerol as a solvent

We describe here a metal and base-free straightforward method to access arylselanyl anilines using glycerol as a solvent. Starting from N,N-disubstituted anilines and arylselanyl chloride, the protocol is general and was successfully applied to a sort of anilines with different substitution patterns in both the aromatic ring and the nitrogen atom. As desirable for a green synthetic procedure, the non-toxic, low volatile, renewable glycerol was used as a solvent at room temperature. This journal is the Partner Organisations 2014.