19989-64-1 Usage
Description
6-Benzothiazolecarboxylic acid, ethyl ester (6CI, 8CI, 9CI), also known as 6-Ethoxycarbonylbenzothiazole, is a chemical compound with the molecular formula C11H9NO2S. It is a pale yellow solid with a molecular weight of 223.26 g/mol. 6-Benzothiazolecarboxylicacid,ethylester(6CI,8CI,9CI) is commonly used as an intermediate in the synthesis of various products and has been studied for its potential applications in organic electronics, material science, and therapeutic effects. However, it is important to handle this compound with care, as it may pose hazards to human health and the environment.
Uses
Used in Pharmaceutical Industry:
6-Benzothiazolecarboxylic acid, ethyl ester (6CI, 8CI, 9CI) is used as an intermediate in the synthesis of pharmaceuticals for its potential therapeutic effects. Its unique chemical structure allows it to be incorporated into various drug molecules, enhancing their properties and efficacy.
Used in Agrochemical Industry:
In the agrochemical industry, 6-Benzothiazolecarboxylic acid, ethyl ester (6CI, 8CI, 9CI) is utilized as an intermediate in the production of agrochemicals. Its chemical properties make it suitable for the development of compounds that can protect crops from pests and diseases, thus ensuring a stable food supply.
Used in Dye Industry:
6-Benzothiazolecarboxylic acid, ethyl ester (6CI, 8CI, 9CI) is used as an intermediate in the synthesis of dyes due to its ability to impart color to various materials. Its chemical structure allows for the creation of dyes with specific color characteristics, making it valuable in the production of textiles, paints, and other color-based products.
Used in Organic Electronics:
6-Benzothiazolecarboxylic acid, ethyl ester (6CI, 8CI, 9CI) has been studied for its potential applications in organic electronics. Its unique properties make it a promising candidate for use in the development of organic light-emitting diodes (OLEDs), organic solar cells, and other electronic devices that rely on organic materials.
Used in Material Science:
In the field of material science, 6-Benzothiazolecarboxylic acid, ethyl ester (6CI, 8CI, 9CI) is being investigated for its potential use in the development of new materials with unique properties. Its chemical structure allows for the creation of materials with enhanced properties, such as improved conductivity, stability, or mechanical strength.
Check Digit Verification of cas no
The CAS Registry Mumber 19989-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,8 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19989-64:
(7*1)+(6*9)+(5*9)+(4*8)+(3*9)+(2*6)+(1*4)=181
181 % 10 = 1
So 19989-64-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO2S/c1-2-13-10(12)7-3-4-8-9(5-7)14-6-11-8/h3-6H,2H2,1H3
19989-64-1Relevant articles and documents
Generation of a thiazole o-quinodimethane from an imino derivative and its intermolecular Diels-Alder trapping with alkynes or quinones
Jouve, Karine,Pautet, Felix,Domard, Monique,Fillion, Houda
, p. 1064 - 1067 (1999)
(E)-5-(N-Benzylformimidoyl)-4-methylthiazole 3 was prepared in good yield from 5-formyl-4-methylthiazole and benzylamine. Treatment of 3 with methylchloroformate in the presence of ethyldiisopropylamine in refluxing toluene has generated o-quinodimethane
Deaminizing method for amidogen-containing aromatic compounds
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Paragraph 0021, (2016/10/09)
The invention relates to the technical field of organic synthesis, and provides a deaminizing method for amidogen-containing aromatic compounds. The deaminizing method aims at solving the problems that as for a deaminizing method commonly used at present, as strong acid is used, the environment is polluted, the reaction temperature needs to be accurately controlled and production is not facilitated. The deaminizing method for the amidogen-containing aromatic compounds includes the steps that the amidogen-containing aromatic compounds, nitrite and solvents are mixed to be put into a pressure-proof tube, a stirring reaction is carried out for 12 hours to 72 hours at the temperature of 80 DEG C to 130 DEG C, and the deaminized-amidogen aromatic compounds are separated and obtained. The deaminizing method is efficient, easy and convenient to operate and free of waste acid pollution.
New analogs of nitrobenzylthioinosine
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Page/Page column 29-30, (2010/11/29)
This invention relates to new analogs or derivatives of nitrobenzylthioinosine, use of these new analogs of nitrobenzylthioinosine for the treatment of pain and various other diseases as well as pharmaceuticals comprising at least on new analog of nitrobenzylthioinosine.
