62652-30-6

Basic information

• Product Name: 2-(ethylsulfanyl)-1,3-benzoxazole
• CAS NO: 62652-30-6
• Molecular Formula: C₉H₉NOS
• Molecular Weight: 179.2389
• Mol File: 62652-30-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 285.2°C at 760 mmHg
• Flash Point: 126.3°C
• Density: 1.22g/cm³
• Vapor Pressure: 0.00488mmHg at 25°C
• Refractive Index: 1.627
• CAS DataBase Reference: 2-(ethylsulfanyl)-1,3-benzoxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(ethylsulfanyl)-1,3-benzoxazole(62652-30-6)
• EPA Substance Registry System: 2-(ethylsulfanyl)-1,3-benzoxazole(62652-30-6)

Safety Data

• Hazardous Substances Data: 62652-30-6(Hazardous Substances Data)

Usage

Chemical structure

2-(ethylsulfanyl)-1,3-benzoxazole is a heterocyclic organic compound consisting of a benzene ring fused to an oxazole ring with an ethylsulfanyl substituent attached at the 2-position.

Family

It belongs to the benzoxazole family.

Properties

2-(ethylsulfanyl)-1,3-benzoxazole has diverse biological and chemical properties, including potential antimicrobial, antiviral, and anti-cancer properties.

Applications

It has potential applications in pharmaceuticals, agrochemicals, and material sciences.

Use as building block

It can be used as a building block in the synthesis of various complex organic molecules.

Subject of interest

It is a subject of interest for further research and development due to its potential biological activities.

Upstream product

• 2382-96-9 benzo[d]oxazole-2-(3H)-thione 
• 74-96-4 ethyl bromide 
• 75-03-6 ethyl iodide 
• 36993-70-1 bis(2-benzoxazolyl) disulfide 
• 122-52-1 triethyl phosphite 
• 122-51-0 orthoformic acid triethyl ester 
• 2382-96-9 2-sulfanyl-1,3-benzoxazole 
• 814-49-3 diethyl chlorophosphate 
• 17073-22-2 N-allyl-N'-(2-hydroxy-phenyl)-thiourea 
• 95-55-6 2-amino-phenol 
• 273-53-0 benzoxazole 
• 75-08-1 ethanethiol 
• 60683-30-9 ethyl N,N′-diisopropylcarbamimidate 

Downstream Products

• 15719-64-9 methylammonium carbonate 
• 95-55-6 2-amino-phenol 
• 75-08-1 ethanethiol 
• 59-49-4 2-hydroxybenzoxazole 
• 59-49-4 2-Benzoxazolinone 
• 6263-62-3 benzyl(ethyl)sulfane 
• 106018-80-8 ethyl-2-(1-naphtyl)ethyl sulfide 
• 66910-82-5 2-(phenethyloxy)benzoxazole 
• 22914-08-5 <2-(ethylthio)ethyl>benzene 

Relevant articles and documents

A novel synthesis of 2-alkylthiobenzothiazoles and 2-alkylthiobenzoxazoles

3H-Benzothiazole-2-thione and 3H-benzoxazole-2-thione were selectively S-alkylated by use of O-alkylisoureas as the alkylating reagents. The reactions could be performed under mild reaction conditions in short reaction times, and high yields were obtained using O-primary-alkylisoureas, whereas low yields were obtained with sec-and tert-alkylisoureas.

One-Flask Synthesis of Sulfides from Alcohols and Alkyl Halides Using Benzoxazoline-2-thione

The synthesis of sulfides from alcohols and benzoxazoline-2-thione (I) was studied to establish its generality and the mechanism of the reaction.A one-flask synthesis of sulfides from alcohols was developed.According to this procedure, various sulfides were prepared without the use of illsmelling thiols.Moreover, partial sulfenylation of diols to give sulfenyl alcohols was achieved.Keywords - one-flask synthesis; benzoxazoline-2-thione; partial sulfenylation; sulfide; sulfenyl alcohol