52754-56-0

Basic information

• Product Name: Benzene, 1-chloro-4-(ethylseleno)-
• CAS NO: 52754-56-0
• Molecular Formula: C8H9ClSe
• Molecular Weight: 219.572
• Mol File: 52754-56-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzene, 1-chloro-4-(ethylseleno)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-chloro-4-(ethylseleno)-(52754-56-0)
• EPA Substance Registry System: Benzene, 1-chloro-4-(ethylseleno)-(52754-56-0)

Safety Data

• Hazardous Substances Data: 52754-56-0(Hazardous Substances Data)

Upstream product

• 93-89-0 benzoic acid ethyl ester 
• 20541-49-5 bis(p-chlorophenyl) diselenide 
• 87136-88-7 p-chlorophenyl isopropyl selenide 
• 106-46-7 para-dichlorobenzene 
• 74-96-4 ethyl bromide 
• 37773-29-8 4-chlorophenyl methyl selenide 
• 75-03-6 ethyl iodide 

Downstream Products

• 57878-20-3 p-chlorobenzeneselenenyl chloride 
• 20541-49-5 bis(p-chlorophenyl) diselenide 
• 20753-53-1 4-chlorobenzeneseleninic acid 
• 856129-18-5 ethyl-dichloro-(4-chloro-phenyl)-λ⁴-selane 

Relevant articles and documents

Production of Alkyl Aryl Sulfides from Aromatic Disulfides and Alkyl Carboxylates via a Disilathiane–Disulfide Interchange Reaction

The results of this study show that disilathiane is an effective mediator in the synthesis of alkyl aryl sulfides with disulfides and alkyl carboxylates. Mechanistic studies suggest that disilathiane promotes cleavage of the sulfur–sulfur bond of disulfides to generate thiosilane as a key intermediate. Diselenides were also applicable to this transformation to produce the corresponding selenides.