6265-92-5

Basic information

• Product Name: 2-(4-METHOXYPHENYL)BENZOTHIAZOLE
• Synonyms: 2-(4-methoxyphenyl)-benzothiazol;2-(p-methoxyphenyl)benzothiazole;2-(4-METHOXYPHENYL)BENZOTHIAZOLE;1-(2-BENZOTHIAZOLYL)-4-METHOXYBENZENE;4-(2-BENZOTHIAZOLYL)ANISOLE;AKOS BBS-00007335;Benzothiazole, 2-(4-methoxyphenyl)-;Benzothiazole, 2-(p-methoxyphenyl)- (6ci,7ci,8ci)
• CAS NO: 6265-92-5
• Molecular Formula: C₁₄H₁₁NOS
• Molecular Weight: 241.31
• Mol File: 6265-92-5.mol
• Article Data: 329

Chemical Properties

• Melting Point: 120.0 to 124.0 °C
• Boiling Point: 392.5 °C at 760 mmHg
• Flash Point: 191.2 °C
• Appearance: /
• Density: 1.234 g/cm³
• Vapor Pressure: 5.16E-06mmHg at 25°C
• Refractive Index: 1.656
• Solubility: soluble in Toluene
• CAS DataBase Reference: 2-(4-METHOXYPHENYL)BENZOTHIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-METHOXYPHENYL)BENZOTHIAZOLE(6265-92-5)
• EPA Substance Registry System: 2-(4-METHOXYPHENYL)BENZOTHIAZOLE(6265-92-5)

Safety Data

• RTECS: DL5330000
• Hazardous Substances Data: 6265-92-5(Hazardous Substances Data)

Usage

General Description

2-(4-Methoxyphenyl)benzothiazole is a chemical compound that belongs to the benzothiazole family. It is commonly used as a fluorescent dye and has applications in various fields such as polymer science, biochemistry, and organic synthesis. The compound is known for its distinctive yellow-green fluorescence and is often utilized as a fluorescent tracer in biological and environmental studies. It is also used as a building block in the synthesis of other organic compounds and has been studied for its potential use in medical imaging and diagnostic applications. Additionally, 2-(4-Methoxyphenyl)benzothiazole has been investigated for its potential anti-inflammatory and antioxidant properties.

InChI:InChI=1/C14H11NOS/c1-16-11-8-6-10(7-9-11)14-15-12-4-2-3-5-13(12)17-14/h2-9H,1H3

Upstream product

• 3585-93-1 N-(4-methoxybenzylidene)aniline oxide 
• 2516-40-7 2-bromo-1,3-benzothiazole 
• 5720-07-0 4-methoxyphenylboronic acid 
• 100-52-7 benzaldehyde 
• 123-11-5 4-methoxy-benzaldehyde 
• 615-43-0 2-iodophenylamine 
• 59118-33-1 1-methoxy-4-triethoxymethyl-benzene 
• 137-07-5 2-amino-benzenethiol 
• 95-16-9 1,3-Benzothiazole 
• 637-69-4 4-Methoxystyrene 
• 19013-30-0 p-methoxyphenyl mesylate 
• 150-76-5 4-methoxy-phenol 
• 1612227-89-0 N-(2-iodophenyl)-4-methoxybenzothioamide 
• 62-53-3 aniline 

Downstream Products

• 1299483-59-2 4-(benzo[d]thiazol-2-yl)phenyl 4-(decyloxy)benzoate 
• 1299483-58-1 4-(benzo[d]thiazol-2-yl)phenyl 4-(octyloxy)benzoate 
• 1454287-81-0 (2-(benzo[d]thiazol-2-yl)-5-methoxyphenyl)(phenyl)methanone 
• 1610358-01-4 Ir(4-Me-2,3-dpq)2(pbt-OMe) 
• 1610357-99-7 Ir(pbt-OMe)2(4-Me-2,3-dpq) 
• 1454287-82-1 2-(benzo[d]thiazol-2-yl)-5-methoxy-1,3-phenylenebis(phenylmethanone) 

Relevant articles and documents

Novel synthesis of 2-arylbenzothiazoles mediated by ceric ammonium nitrate (CAN).

[reaction: see text] Cyclization of the intermediate radical formed after initial oxidative coupling between thiophenols and aromatic nitriles leads to the synthesis of a wide range of 2-arylbenzothiazoles.

A biomass-derived N-doped porous carbon catalyst for the aerobic dehydrogenation of nitrogen heterocycles

N-doped porous carbon (NC) was synthesized from sugar cane bagasse, which is a sustainable and widely available biomass waste. The preferred NC sample had a well-developed porous structure, a graphene-like surface morphology and different N species. More

Room temperature HFIP/Ag-promoted palladium-catalyzed C–H functionalization of benzothiazole with iodoarenes

A versatile synthetic protocol involving the room temperature direct arylation of benzothiazole with a wide variety of iodoarenes under Ag-promoted Pd-catalyzed conditions in HFIP as the reaction solvent has been presented. A sequential HFIP-promoted sele