29647-76-5

Basic information

• Product Name: (naphth-1-ylamino)phenoxymethane-1-thione
• Synonyms: (naphth-1-ylamino)phenoxymethane-1-thione
• CAS NO: 29647-76-5
• Molecular Weight: 279.362
• Mol File: 29647-76-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (naphth-1-ylamino)phenoxymethane-1-thione(CAS DataBase Reference)
• NIST Chemistry Reference: (naphth-1-ylamino)phenoxymethane-1-thione(29647-76-5)
• EPA Substance Registry System: (naphth-1-ylamino)phenoxymethane-1-thione(29647-76-5)

Safety Data

• Hazardous Substances Data: 29647-76-5(Hazardous Substances Data)

Upstream product

• 134-32-7 1-amino-naphthalene 
• 1005-56-7 phenylcarbonochloridothioate 

Downstream Products

• 24775-57-3 1-naphthalen-1-yl-3-phenyl-thiourea 
• 107544-71-8 1-benzyl-3-(naphthalen-1-yl)thiourea 
• 551-06-4 1-isothiocyanatonaphthalene 

Relevant articles and documents

Convenient synthesis of unsymmetrical N,N′-disubstituted thioureas in water

A simple and convenient two-step method has been developed and used to synthesise 25 (4 of which are novel) unsymmetrical N,N′-disubstituted thioureas in water. Alkylamines or variously substituted arylamines reacted smoothly with phenyl chlorothionoformate at room temperature to form thiocarbamates, which were then reacted with another alkyl- or arylamine in water at reflux to afford the unsymmetrical N,N′-disubstituted thioureas in good to excellent yields. Mild conditions, simple work-up, high yields as well as using water as solvent are the major advantages of the method.

Preparation of aryl isothiocyanates via protected phenylthiocarbamates and application to the synthesis of caffeic acid (4-isothiocyanato)phenyl ester

-