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5-Benzothiazolecarboxylic acid, ethyl ester (6CI, 9CI), is a chemical compound belonging to the benzothiazolecarboxylic acid esters class. It is characterized by its molecular formula C11H9NO2S and a molecular weight of 223.26 g/mol. This versatile compound is known for its applications in the synthesis of pharmaceuticals, agrochemicals, and dyes, as well as for its potential anticancer and antimicrobial properties. Its ethyl ester form enhances its solubility and ease of handling in various chemical reactions, making it a valuable asset in synthetic chemistry.

103261-70-7

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103261-70-7 Usage

Uses

Used in Pharmaceutical Industry:
5-Benzothiazolecarboxylic acid, ethyl ester (6CI, 9CI) is used as a building block in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 5-Benzothiazolecarboxylic acid, ethyl ester (6CI, 9CI) serves as a key component in the creation of agrochemicals, aiding in the development of products designed to protect crops and enhance agricultural productivity.
Used in Dye Industry:
5-Benzothiazolecarboxylic acid, ethyl ester (6CI, 9CI) is utilized in the dye industry as a crucial intermediate in the production of various dyes, contributing to the coloration and performance of these products.
Used in Anticancer Applications:
5-Benzothiazolecarboxylic acid, ethyl ester (6CI, 9CI) is employed as a potential anticancer agent, leveraging its reported anticancer properties to contribute to the development of novel treatments for various types of cancer.
Used in Antimicrobial Applications:
5-Benzothiazolecarboxylicacid,ethylester(6CI,9CI) is also used in antimicrobial applications, capitalizing on its antimicrobial properties to develop products that can combat microbial infections and contribute to public health.
Used in Laboratory Research and Diagnostic Applications:
5-Benzothiazolecarboxylic acid, ethyl ester (6CI, 9CI) is used as a fluorescence indicator in laboratory research and diagnostic applications, providing a valuable tool for visualizing and studying various biological processes and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 103261-70-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,2,6 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103261-70:
(8*1)+(7*0)+(6*3)+(5*2)+(4*6)+(3*1)+(2*7)+(1*0)=77
77 % 10 = 7
So 103261-70-7 is a valid CAS Registry Number.

103261-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl benzo[d]thiazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 1,3-benzothiazole-5-carboxylate

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:103261-70-7 SDS

103261-70-7Relevant articles and documents

Generation and Diels-Alder trapping of 4,5-bis(bromomethylene)-4,5-dihydrothiazole

Jouve, Karine,Pautet, Felix,Domard, Monique,Fillion, Houda

, p. 2047 - 2050 (1998)

Treatment of 4,5-bis(dlbromomethyl)thiazole (1a) with sodium iodide in DMF led to 4,5-bis(bromomethylene)-4,5-dihydrothiazole (2a). Trapping the latter in situ with dienophiles afforded directly the aromatized cycloadducts. Starting with 5-hydroxynaphthoquinone or its 2- and 3-bromo derivatives 6 gave a mixture of the tetracyclic quinones 10 + 11 from which the 1,6-regioisomer 10 predominates. Using acrylate dienophiles gave 6-substituted benzothiazoles 13 as the major products. The regiochemistry of the cycloadditions between 2a and naphthoquinones 6 agrees with the predictions of the frontier molecular orbital theory. In contrast, the regioselectivity observed from 2a and acrylate dienophiles 12, similar to that previously obtained with 5-bromomethylene-4-methylene-4,5-dihydrothiazole (2b), is opposite to that predicted and could be better accomodated by a competitive Michael addition followed by a cyclization-elimination step.

INDAZOLES, BENZOTHIAZOLES, BENZOISOTHIAZOLES, BENZISOXAZOLES, AND PREPARATION AND USES THEREOF

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Page/Page column 70-71, (2010/02/14)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nACh receptors), activation of nACh receptors, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (e.g., indazoles and benzothiazoles), which act as ligands for the α7 nACh receptor subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

ANABASEINE DERIVATIVES USEFUL IN THE TREATMENT OF NEURODEGENERATIVE DISEASES

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Page/Page column 79, (2008/06/13)

The compounds of the present invention are of formula (I): wherein A, R3, R4 is as defined herein, are useful as ligands for nicotinic receptors.

INDAZOLES, BENZOTHIAZOLES, AND BENZOISOTHIAZOLES, AND PREPARATION AND USES THEREOF

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Page 105;106, (2008/06/13)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nAChR), activation of nAChRs, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (indazoles and benzothiazoles), which act as ligands for the α7 nAChR subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

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