6265-92-5

Usage

Uses

Used in Research and Development:
2-(4-Methoxyphenyl)benzothiazole is used as a fluorescent dye for its yellow-green fluorescence, which aids in the visualization and tracking of molecules in biological and environmental studies.
Used in Polymer Science:
In the polymer industry, 2-(4-Methoxyphenyl)benzothiazole is used as a building block in the synthesis of other organic compounds, contributing to the development of new materials with specific properties.
Used in Biochemistry:
2-(4-Methoxyphenyl)benzothiazole serves as a fluorescent tracer in biochemistry, enabling researchers to study molecular interactions and processes within biological systems.
Used in Organic Synthesis:
As a key component in organic synthesis, 2-(4-Methoxyphenyl)benzothiazole is utilized to create a variety of organic compounds with diverse applications.
Used in Medical Imaging and Diagnostics:
2-(4-Methoxyphenyl)benzothiazole is being investigated for its potential use in medical imaging and diagnostics, where its fluorescent properties could enhance the detection and monitoring of diseases.
Used in Pharmaceutical Development:
2-(4-METHOXYPHENYL)BENZOTHIAZOLE has been studied for its potential anti-inflammatory and antioxidant properties, indicating its possible use in the development of pharmaceuticals for treating inflammation and oxidative stress-related conditions.

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

• 3292-42-0 2-aminobenzenethiol hydrochloride 
• 123-11-5 4-methoxy-benzaldehyde 
• 137-07-5 2-amino-benzenethiol 
• 26060-23-1 4-methoxy-N-phenylthiobenzamide 
• 58249-76-6 bis[2-(4-anisoylamino)phenyl] disulfide 
• 100-07-2 4-methoxy-benzoyl chloride 
• 105-64-6 diisopropyl peroxydicarbonate 
• 142505-39-3 N-(4-methoxyphenylmethylene)-2-methylthiobenzenamine 
• 3585-93-1 N-(4-methoxybenzylidene)aniline oxide 
• 76148-60-2 3-(4-methoxyphenyl)-2H-benzo[b][1,4]thiazin-2-one 
• 874-90-8 4-methoxybenzonitrile 
• 39145-31-8 2-cyano-3-(4-methoxyphenyl)thioacrylamide 
• 100-09-4 4-methoxybenzoic acid 
• 1155-00-6 bis(2-nitrophenyl)disulfide 

Downstream Products

• 1454287-81-0 (2-(benzo[d]thiazol-2-yl)-5-methoxyphenyl)(phenyl)methanone 
• 1454287-82-1 2-(benzo[d]thiazol-2-yl)-5-methoxy-1,3-phenylenebis(phenylmethanone) 
• 53544-77-7 2-(4-methoxy-phenyl)-benzothiazol-6-ylamine 
• 6265-55-0 2-(4-hydroxyphenyl)benzothiazole 
• 53544-70-0 2-(4-methoxyphenyl)-6-nitrobenzothiazole 
• 21223-49-4 N-methyl-2-(4-methoxyphenyl)benzothiazolium iodide 
• 1610358-01-4 Ir(4-Me-2,3-dpq)2(pbt-OMe) 
• 1610357-99-7 Ir(pbt-OMe)2(4-Me-2,3-dpq) 
• 90481-46-2 2-(2'-Hydroxy-4'-methoxyphenyl)benzothiazole 
• 1379479-41-0 2-(5'-methoxy-[1,1':3',1''-terphenyl]-2'-yl)benzo[d]thiazole 

Relevant academic research and scientific papers

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.

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

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

Recyclable copper-catalyzed cyclization of o-haloanilides and metal sulfides: An efficient and practical access to substituted benzothiazoles

An efficient heterogeneous copper-catalyzed cyclization of o-haloanilides and metal sulfides has been achieved via the C–S coupling in DMF at 80 or 140 °C in the existence of an MCM-41-bound NHC-Cu(I) catalyst and then intramolecular condensation, delivering a wide range of substituted benzothiazoles in mostly good to high yields. This new MCM-41-NHC-CuI complex can facilely be obtained by a two-step procedure starting from easily accessible and inexpensive reagents and reused more than seven times without any significant loss of its catalytic efficiency. The present protocol has been successfully applied to the gram-scale synthesis of two antitumor agents 5F203 and PMX 610.

RADIOLABELED COMPOUNDS

This invention relates to radiolabelled compounds as described herein, precursor compounds and reference compounds, as well as pharmaceutical compositions comprising the radiolabelled compounds, which are for use in a diagnostic method practised on the hu

Visible-Light Carbon Nitride-Catalyzed Aerobic Cyclization of Thiobenzanilides under Ambient Air Conditions

A metal-free heterogeneous photocatalysis has been developed for the synthesis of benzothiazoles via intramolecular C-H functionalization/C-S bond formation of thiobenzanilides by inexpensive graphitic carbon nitride (g-C3N4) under visible-light irradiation. This reaction provides access to a broad range of 2-substituted benzothiazoles in high yields under an air atmosphere at room temperature without addition of a strong base or organic oxidizing reagents. In addition, the catalyst was found to be stable and reusable after five reaction cycles.

An efficient rapid synthesis of benzoxazoles and benzothiazoles using pma.Sio2 at room temperature under heterogeneous conditions

Treatment of 2-aminophenol (or 2-aminothiophenol) with aromatic aldehydes in the presence of phosphomolybdic acid on silica at room temperature affords the corresponding benzoxazoles (or benzothiazoles) in excellent yields (88-96%) under heterogeneous conditions. Benzoxazoles and benzothiazoles are formed in less than 10 min.

Ultrasound-assisted efficient and green synthesis of 2-substituted benzothiazoles under solvent-free condition using recyclable sulfated tungstate

Sulfated tungstate catalyzed an efficient and ecofriendly protocol has been described for the synthesis of 2-substituted benzothiazoles. The corresponding benzothiazoles were obtained using a condensation reaction of 2-aminothiophenol with various aldehydes under ultrasound irradiation at room temperature. Various functional groups on the 2-aminothiophenol as well as on the aldehydes were tolerated to provide 2-substituted benzothiazoles derivatives in excellent yields. The faster reaction rate, solvent-free or mild reaction conditions, wide functional group compatibility, excellent yields, easy work-up procedure, and excellent catalyst recyclability are the advantages of this protocol. These advantages make this process more practicable, cost-effective, and environmentally benign.

Fast and high-efficiency synthesis of 2-substituted benzothiazoles via combining enzyme catalysis and photoredox catalysis in one-pot

An efficient and green method, combining enzymatic and visible-light catalysis for synthesis of the widely applicable 2-substituted benzothiazoles, has been developed. This method features a relay catalysis protocol consisting of biocatalytic promiscuity

Ruthenium silicate (RS-1) zeolite: novel heterogeneous efficient catalyst for synthesis of 2-arylbenzothiazole derivatives

Abstract: Mesoporous silicate and transition metal (Ru+3) containing mesoporous silicate materials or ruthenium silicate Ru+3/Si+4 where synthesis by using hydrothermal process. Mesoporous ruthenium silicate (RS-1) and zeo