6265-58-3

Basic information

• Product Name: Benzothiazole, 2-(2-ethoxyphenyl)-
• Synonyms: Benzothiazole, 2-(2-ethoxyphenyl)-
• CAS NO: 6265-58-3
• Molecular Formula: C₁₅H₁₃NOS
• Molecular Weight: 255.33
• Mol File: 6265-58-3.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 412.5°C at 760 mmHg
• Flash Point: 203.2°C
• Appearance: /
• Density: 1.204g/cm³
• Vapor Pressure: 1.24E-06mmHg at 25°C
• Refractive Index: 1.64
• CAS DataBase Reference: Benzothiazole, 2-(2-ethoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzothiazole, 2-(2-ethoxyphenyl)-(6265-58-3)
• EPA Substance Registry System: Benzothiazole, 2-(2-ethoxyphenyl)-(6265-58-3)

Safety Data

• Hazardous Substances Data: 6265-58-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H13NOS/c1-2-17-13-9-5-3-7-11(13)15-16-12-8-4-6-10-14(12)18-15/h3-10H,2H2,1H3

Upstream product

• 37806-29-4 2-(ethoxy)benzylamine 
• 137-07-5 2-amino-benzenethiol 
• 613-69-4 2-ethoxylbenzaldehyde 
• 609-73-4 o-nitroiodobenzene 
• 95-16-9 1,3-Benzothiazole 
• 42926-52-3 2-ethoxybenzoyl chloride 

Relevant articles and documents

Syntheses of 2-aryl benzothiazoles via photocatalyzed oxidative condensation of amines with 2-aminothiophenol in the presence of bodipy derivatives

A simple, convenient, and efficient new method for synthesis of 2-aryl benzothiazoles under mild conditions with nonmetal catalyst has been developed. Boron-dipyrromethene (BODIPY) dyes were used as photocatalysts for aerobic oxidative reactions of amine with 2-aminothiophenol. The approach will be very useful for the synthesis of benzothiazole derivatives and the development of photocatalytic reactions.

Synthesis of 2-aryl benzothiazoles via K2S2O 8-mediated oxidative condensation of benzothiazoles with aryl aldehydes

Nontransition metal-catalyzed synthesis of 2-aryl benzothiazoles was achieved through K2S2O8-mediated oxidative condensation of benzothiazoles with aryl aldehydes. The same transformation can also be effected when the aryl

Control of acarids using certain benzothiazoles or benzothiazolines

Compounds having either of the structures SPC1 Have strong acaricidal activity, in which R is a phenyl or naphthyl group, or phenyl with certain designated substitution. Thus, mites may be controlled on such crops as cotton by applying such compounds as 2-(1-naphthyl)benzothiazoline or 2-(5-t-butyl-2-hydroxyphenyl)benzothiazole.