6265-89-0

Basic information

• Product Name: 2-(3,4-Dichloro-phenyl)-benzothiazole
• Synonyms: 2-(3,4-Dichloro-phenyl)-benzothiazole
• CAS NO: 6265-89-0
• Molecular Formula: C₁₃H₇Cl₂NS
• Molecular Weight: 280.17
• Mol File: 6265-89-0.mol
• Article Data: 19

Chemical Properties

• Boiling Point: 417.9°C at 760 mmHg
• Flash Point: 206.5°C
• Appearance: /
• Density: 1.433g/cm³
• Vapor Pressure: 8.3E-07mmHg at 25°C
• Refractive Index: 1.693
• CAS DataBase Reference: 2-(3,4-Dichloro-phenyl)-benzothiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,4-Dichloro-phenyl)-benzothiazole(6265-89-0)
• EPA Substance Registry System: 2-(3,4-Dichloro-phenyl)-benzothiazole(6265-89-0)

Safety Data

• Hazardous Substances Data: 6265-89-0(Hazardous Substances Data)

Usage

Benzothiazole derivative

A chemical compound derived from benzothiazole, with modifications to its structure, in this case, the addition of two chlorine atoms attached to the phenyl ring.

Two chlorine atoms attached to the phenyl ring

The presence of two chlorine atoms covalently bonded to the phenyl ring, which can influence the compound's properties and reactivity.

Widely used in rubber and plastic materials

This chemical compound is commonly employed in the production of rubber and plastic materials, contributing to their properties and performance.

Anti-aging agent

It serves as an anti-aging agent, helping to prevent the degradation of rubber and plastic materials over time, thus extending their lifespan.

Fluorescent dye

The compound can be used as a fluorescent dye, imparting bright and visible colors to various materials.

Pesticide

2-(3,4-Dichloro-phenyl)-benzothiazole has pesticidal properties, making it useful for controlling pests in agricultural and other settings.

Potential skin and eye irritation

This chemical compound may cause irritation to the skin and eyes, necessitating proper handling and protective measures.

Harmful if swallowed or inhaled

Ingestion or inhalation of 2-(3,4-Dichloro-phenyl)-benzothiazole may be harmful to human health, so it is essential to follow safety guidelines and minimize exposure.

InChI:InChI=1/C13H7Cl2NS/c14-9-6-5-8(7-10(9)15)13-16-11-3-1-2-4-12(11)17-13/h1-7H

Upstream product

• 98370-54-8 zinc 2-aminobenzenethiolate 
• 6287-38-3 3,4-dichlorobenzaldehyde 
• 137-07-5 2-amino-benzenethiol 
• 3024-72-4 3,4-dichlorobenzoyl chloride 
• 95-16-9 1,3-Benzothiazole 
• 20555-91-3 3,4-dichloroiodobenzene 
• 1239970-45-6 C₂₆H₁₆Cl₄N₂S₂ 
• 102-49-8 3,4-dichlorobenzyl amine 
• 51-44-5 3,4-dichlorbenzoic acid 
• 5807-30-7 3,4-dichlorophenyl acetic acid 
• 615-43-0 2-iodophenylamine 
• 95-75-0 3,4-Dichlorotoluene 

Relevant articles and documents

Photoinduced Heterogeneous C?H Arylation by a Reusable Hybrid Copper Catalyst

Heterogeneous copper catalysis enabled photoinduced C?H arylations under exceedingly mild conditions at room temperature. The versatile hybrid copper catalyst provided step-economical access to arylated heteroarenes, terpenes and alkaloid natural products with various aryl halides. The hybrid copper catalyst could be reused without significant loss of catalytic efficacy. Detailed studies in terms of TEM, HRTEM and XPS analysis of the hybrid copper catalyst, among others, supported its outstanding stability and reusability.

Elemental Sulfur-Mediated Decarboxylative Redox Cyclization Reaction: Copper-Catalyzed Synthesis of 2-Substituted Benzothiazoles

A S 8 -mediated directed decarboxylative redox-cyclization strategy for the synthesis of 2-substituted benzothiazoles from o -iodoanilines, arylacetic acids, and elemental sulfur catalyzed by cheap copper metal has been developed. This reaction is operationally simple, ligand-free, compatible with a wide range of functional groups, and provides the desired products in good to excellent yields. In addition, a gram-scale experiment was carried out to furnish PMX 610, an antitumor drug.

The immunomodulation potential of the synthetic derivatives of benzothiazoles: Implications in immune system disorders through in vitro and in silico studies

Benzothiazole and its natural or synthetic derivatives have been used as precursors for several pharmacological agents for neuroprotective, anti-bacterial, and anti-allergic activities. The objecctive of the present study was to evaluate effects of benzot