1286990-00-8

Basic information

• Product Name: ethyl 4-((phenylsulfonyl)oxy)benzoate
• Synonyms: ethyl 4-((phenylsulfonyl)oxy)benzoate
• CAS NO: 1286990-00-8
• Molecular Weight: 306.339
• Mol File: 1286990-00-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl 4-((phenylsulfonyl)oxy)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 4-((phenylsulfonyl)oxy)benzoate(1286990-00-8)
• EPA Substance Registry System: ethyl 4-((phenylsulfonyl)oxy)benzoate(1286990-00-8)

Safety Data

• Hazardous Substances Data: 1286990-00-8(Hazardous Substances Data)

Upstream product

• 120-47-8 Ethyl 4-hydroxybenzoate 
• 873-55-2 sodium benzenesulfonate 
• 98-09-9 benzenesulfonyl chloride 

Downstream Products

• 63676-19-7 [6-methoxy-2-(4-methoxyphenyl)benzo[b]thiophen-3-yl](4-hydroxyphenyl)methanone 
• 1293362-49-8 benzenesulfonic acid-4-[6-methoxy-2-(4-methoxy-phenyl)-benzo[b]thiophene-3-carbonyl]-phenyl ester 
• 1293362-39-6 Sodium 4-[6-methoxy-2-(4-methoxy-phenyl)-benzo[b]thiophene-3-carbonyl]-phenolate 
• 1293362-40-9 Potassium 4-[6-methoxy-2-(4-methoxy-phenyl)-benzo[b]thiophene-3-carbonyl]-phenolate 
• 7507-41-7 4-benzenesulfonyloxy-benzoic acid 
• 84541-36-6 [2-(4-methoxyphenyl)-6-methoxybenzo[b]thien-3-yl][4-[2-(1-piperidinyl)ethoxy]phenyl]methanone hydrochloride 
• 84541-38-8 [6-Methoxy-2-(4-Methoxyphenyl)benzo[b]thien-3-yl]-[4-[2-(1-Piperidinyl)ethoxy]phenyl] Methanone 
• 1293362-54-5 1-(2-{4-[6-Methoxy-2-(4-methoxy-phenyl)-benzo[b]thiophene-3-carbonyl]-phenoxy}-ethyl)-piperidinium bromide 
• 1293408-87-3 1-(2-(4-[6-Hydroxy-2-(4-hydroxy-phenyl)-benzo[b]thiophene-3-carbonyl]-phenoxy)-ethyl)-piperidinium bromide 
• 195062-62-5 ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 
• 85100-62-5 4-n-butylbenzoic acid ethyl ester 
• 93-89-0 benzoic acid ethyl ester 
• 82640-04-8 raloxifene hydrochloride 

Relevant articles and documents

Practical Electro-Oxidative Sulfonylation of Phenols with Sodium Arenesulfinates Generating Arylsulfonate Esters

A practical and sustainable synthesis of arylsulfonate esters has been developed through electro-oxidation. This reaction employed the stable and readily available phenols and sodium arenesulfinates as the starting materials and took place under mild reaction conditions without additional oxidants. A wide range of arylsulfonate esters including those bearing functional groups were produced in good to excellent yields. This reaction could also be conducted at a gram scale without a decrease of reaction efficiency. Those results well demonstrated the potential synthetic value of this reaction in organic synthesis.

A PROCESS FOR PREPARING BENZO[B]THIOPHENE DERIVATIVES

The present invention relates in general to the field of organic chemistry, and in particular to the preparation of benzo[b]thiophene derivatives. These benzo[b]thiophene derivatives are useful as intermediates in the synthesis of pharmaceutically active agents such as raloxifene or derivatives thereof.