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2-(2,3-dimethoxyphenyl)-1,3-benzothiazole is a chemical compound with the molecular formula C15H13NO2S. It is a derivative of benzothiazole, a heterocyclic compound consisting of a benzene ring fused to a thiazole ring. The compound features a 2,3-dimethoxyphenyl group attached to the benzothiazole core, which contributes to its unique chemical properties. This organic molecule is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its ability to form stable complexes and its electronic properties. The compound's structure and functional groups make it a subject of interest for researchers exploring new compounds with specific biological activities or material properties.

6265-59-4

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6265-59-4 Usage

Chemical structure

2-(2,3-dimethoxyphenyl)-1,3-benzothiazole, also known as DMOPBT.

Physical form

Yellowish powder.

Uses

Manufacturing of dyes, pharmaceuticals, and as a fluorescence probe in biochemical assays.

Potential use

Organic light-emitting diodes (OLEDs) due to high electron mobility and good film-forming properties.

Health-related properties

Antioxidant and anti-inflammatory properties, making it a potential candidate for pharmaceutical applications.

Additional information

Further research is needed to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 6265-59-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6265-59:
(6*6)+(5*2)+(4*6)+(3*5)+(2*5)+(1*9)=104
104 % 10 = 4
So 6265-59-4 is a valid CAS Registry Number.

6265-59-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,3-dimethoxyphenyl)-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6265-59-4 SDS

6265-59-4Downstream Products

6265-59-4Relevant academic research and scientific papers

Lawesson's reagent and microwaves: A new efficient access to benzoxazoles and benzothiazoles from carboxylic acids under solvent-free conditions

Seijas, Julio A.,Vázquez-Tato, M. Pilar,Carballido-Reboredo, M. Raquel,Crecente-Campo, José,Romar-López, Lucía

, p. 313 - 317 (2007/10/03)

Lawesson's reagent acts as an efficient promoter in the solvent-free microwave-assisted synthesis of 2-substituted benzoxazoles from carboxylic acids and 2-aminophenol, and thus, constitutes a general synthetic method for these compounds. This new application of Lawesson's reagent is valid also for benzothiazoles with very high efficiency level. A variety of aromatic, heteroaromatic and aliphatic carboxylic acids react under the conditions developed with good yields in all cases. Thiobenzoic acid is a good alternative for microwave-assisted synthesis of 2-phenylbenzoxazole and 2- phenylbenzothiazole in the absence of solvents. Georg Thieme Verlag Stuttgart.

An efficient acid- and metal-free one-pot synthesis of benzothiazoles from carboxylic acids

Rudrawar, Santosh,Kondaskar, Atul,Chakraborti, Asit K.

, p. 2521 - 2526 (2007/10/03)

Carboxylic acids are converted to benzothiazoles in a one-pot reaction with thionyl chloride followed by treatment with 2-aminothiophenol under acid- and catalyst-free conditions. Georg Thieme Verlag Stuttgart.

An efficient synthesis of benzothiazoles by direct condensation of carboxylic acids with 2-aminothiophenol under microwave irradiation

Chakraborti, Asit K.,Selvam,Kaur, Gurmeet,Bhagat, Srikant

, p. 851 - 855 (2007/10/03)

Carboxylic acids are converted to benzothiazoles by direct condensation with 2-aminothiophenol under microwave irradiation in the absence of solvent.

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