119286-02-1

Basic information

• Product Name: S-naphthalen-1-yl ethanethioate
• Synonyms: S-naphthalen-1-yl ethanethioate
• CAS NO: 119286-02-1
• Molecular Weight: 202.277
• Mol File: 119286-02-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: S-naphthalen-1-yl ethanethioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-naphthalen-1-yl ethanethioate(119286-02-1)
• EPA Substance Registry System: S-naphthalen-1-yl ethanethioate(119286-02-1)

Safety Data

• Hazardous Substances Data: 119286-02-1(Hazardous Substances Data)

Upstream product

• 90-11-9 1-Bromonaphthalene 
• 10387-40-3 potassium thioacetate 
• 28912-93-8 1-naphthyldiazonium tetrafluoroborate 

Downstream Products

• 1069128-02-4 2-benzyl-3-methylnaphtho[1,2-b]thiophene 

Relevant articles and documents

THE REACTIVITY OF SULFUR NUCLEOPHILES TOWARDS ARENEDIAZONIUM TETRAFLUOROBORATES IN APROTIC SOLVENTS: SYNTHESIS OF S-ARYL THIOACETATES

Various S-aryl thioacetates are prepared in 40-60percent yield by treatment of arenediazonium tetrafluoroborates with commercial potassium thioacetate in DMSO at room temperature.

THE REACTION BETWEEN ARENEDIAZONIUM TETRAFLUOROBORATES AND ALKALINE THICARBOXYLATES IN DMSO: A CONVENIENT ACCESS TO ARYL THIOLESTERS AND OTHER AROMATIC SULFUR DERIVATIVES.

The reaction between potassium thioacetate or sodium thiobenzoate and arenediazonium tetrafluoroborates in DMSO leads to the corresponding aryl thiolesters 1 which can either be isolated or further reacted providing a convenient one-pot access to a number of other aromatic sulfur derivatives.