94800-51-8

Basic information

• Product Name: Benzene, 1-chloro-4-(phenylseleno)-
• CAS NO: 94800-51-8
• Molecular Formula: C12H9ClSe
• Molecular Weight: 267.616
• Mol File: 94800-51-8.mol
• Article Data: 39

Chemical Properties

• CAS DataBase Reference: Benzene, 1-chloro-4-(phenylseleno)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-chloro-4-(phenylseleno)-(94800-51-8)
• EPA Substance Registry System: Benzene, 1-chloro-4-(phenylseleno)-(94800-51-8)

Safety Data

• Hazardous Substances Data: 94800-51-8(Hazardous Substances Data)

Upstream product

• 1666-13-3 diphenyl diselenide 
• 1679-18-1 4-Chlorophenylboronic acid 
• 38447-69-7 4-chlorobenzenecarboselenoic acid Se-phenyl ester 
• 108-86-1 bromobenzene 
• 56075-36-6 1-(4-chlorophenyl)-2-(methylsulfonyl)diazene 
• 5707-04-0 Phenylselenyl chloride 
• 1073-70-7 4-chlorophenylhydrazine hydrochloride 
• 106-39-8 bromochlorobenzene 
• 71098-88-9 N-phenylselanylphthalimide 
• 89523-62-6 (4-chlorophenyl)zinc(II) chloride 
• 18255-05-5 benzyl phenyl selenide 
• 20541-49-5 bis(p-chlorophenyl) diselenide 
• 59-88-1 phenylhydrazine hydrochloride 
• 2564-83-2 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical 

Downstream Products

• 127764-10-7 dichloro-(4-chloro-phenyl)-phenyl-λ⁴-selane 

Relevant articles and documents

Trichloroisocyanuric Acid-Promoted Synthesis of Arylselenides and Aryltellurides from Diorganyl Dichalcogenides and Arylboronic Acids at Ambient Temperature

A transition-metal-free method for the synthesis of arylselenides and aryltellurides has been established based on the oxidative cross-coupling between diorganyl dichalcogenides and aryl boronic acids. With trichloroisocyanuric acid as an oxidant, the reaction proceeded smoothly to afford the desired products in 45–97% yields at ambient temperature. Three reaction reagents used in this method are stoichiometric and the oxidation by-product isocyanuric acid can be easily isolated and recovered. Besides of arylboronic acids, aryl trifluoroborates and aryl trihydroxyborates salts are also able to perform this transformation. (Figure presented.).

Photocatalyst-free photoredox synthesis of diaryl selenides by reaction of diselenides with aryldiazo sulfones

A photcatalyst-free photoredox synthesis of diaryl selenides has been developed by coupling reaction of diselenides with aryldiazo sulfones. The reaction was accelerated under visible light irradiation without using a photocatalyst or photosensitizer. This approach facilitates the synthesis of diaryl selendes with a wide range of functional group tolerance.

New routes for the synthesis of unsymmetrical diarylselenides: Effect of heat, light and ultrasound

Herein, we report the photochemical coupling of diphenyldiselenides with substituted phenylhydrazine hydrochloride without catalyst. The protocol was developed not only in presence of sunlight and UV light but also under thermal condition for comparison study. Moreover, ultrasound assisted new catalytic protocol was developed using Ni(II)/L-proline system in DMSO with the advantage of shorter reaction time compared to earlier reports. We have also developed a new C-Se cross coupling reaction where phenylselenyl chloride and arylhydrazine hydrochlorides were effectively coupled using developed catalytic system.