22872-52-2

Basic information

• Product Name: S-ethyl 4-methoxybenzothioate
• Synonyms: S-ethyl 4-methoxybenzothioate
• CAS NO: 22872-52-2
• Molecular Weight: 196.27
• Mol File: 22872-52-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: S-ethyl 4-methoxybenzothioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-ethyl 4-methoxybenzothioate(22872-52-2)
• EPA Substance Registry System: S-ethyl 4-methoxybenzothioate(22872-52-2)

Safety Data

• Hazardous Substances Data: 22872-52-2(Hazardous Substances Data)

Upstream product

• 625-60-5 ethyl thioacetate 
• 201230-82-2 carbon monoxide 
• 696-62-8 para-iodoanisole 
• 28519-30-4 S-ethyl p-toluenethiosulfonate 
• 123-11-5 4-methoxy-benzaldehyde 
• 64-17-5 ethanol 
• 100-09-4 4-methoxybenzoic acid 
• 75599-70-1 C₃H₅OS⁽¹⁺⁾*F₆Sb^(1-) 
• 100-66-3 methoxybenzene 
• 100-07-2 4-methoxy-benzoyl chloride 
• 75-08-1 ethanethiol 

Downstream Products

• 24468-81-3 1-(1-Ethylsulfanyl-2-methyl-propenyl)-4-methoxy-benzene 
• 100-09-4 4-methoxybenzoic acid 
• 75-08-1 ethanethiol 
• 105-13-5 4-Methoxybenzyl alcohol 
• 171364-79-7 2-(4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 5449-69-4 2,4'-dimethoxybenzophenone 

Relevant articles and documents

Nickel-catalyzed carbonylation of thioacetates with aryl iodides via CO insertion and C–S bond cleavage

Aryl thioesters are synthesized via nickel-catalyzed carbonylation of thioacetates with aryl iodides. Alkyl thioacetates undergo coupling with carbon monoxide and aryl iodides to produce the desired aryl thioesters in moderate yields. This catalytic carbonylative coupling process provides a cost-effective and direct approach for the preparation of useful thioesters.

Rhodium-Catalyzed Decarbonylative Borylation of Aromatic Thioesters for Facile Diversification of Aromatic Carboxylic Acids

Transformation of aromatic thioesters into arylboronic esters was achieved efficiently using a rhodium catalyst. The broad functional-group tolerance and mild conditions of the method have allowed for the two-step decarboxylative borylation of a wide range of aromatic carboxylic acids, including commercially available drugs.

Convenient and efficient synthesis of thiol esters using zinc oxide as a heterogeneous and eco-friendly catalyst

A catalytic method was developed to synthesize thiol esters from the reaction of acyl chlorides and thiols using zinc oxide as a catalyst under solvent-free conditions at room temperature. Mild reaction conditions, short reaction time, excellent yields of products and recyclability of the catalyst are noteworthy features of this methodology. CSIRO 2008.