Nombre del producto:5-Chloro-2-benzothiazolinone

IUPAC Name:5-chloro-2,3-dihydro-1,3-benzothiazol-2-one

CAS:20600-44-6
Fórmula molecular:C7H4ClNOS
Pureza:95%+
Número de catálogo:CM156973
Peso molecular:185.63

Unidad de embalaje Stock disponible Precio($) Cantidad
CM156973-25g in stock ưǤ
CM156973-100g in stock ʼnNJĽ

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Detalles del producto

Núm. De CAS :20600-44-6
Fórmula molecular:C7H4ClNOS
Punto de fusión:-
Código de sonrisas:O=C1SC2=CC=C(Cl)C=C2N1
Densidad:
Número de catálogo:CM156973
Peso molecular:185.63
Punto de ebullición:
Nº Mdl:MFCD00060125
Almacenamiento:Store at 2-8°C.

Category Infos

Benzothiazoles
Benzothiazoles are aromatic heterocyclic compounds with the chemical formula C7H5NS. Benzothiazoles and their derivatives are a very important class of heterocyclic compounds that are ubiquitous in nature and are mainly used in medicine, agriculture and industry. In medicine, benzothiazole derivatives are a kind of very important pharmaceutical intermediates with good pharmacological and biological activities. It can be used as a fungicide, anti-tuberculosis drug, anti-malarial, anti-convulsant, insecticide, sedative and anti-inflammatory drug, and can also be used to treat diabetes and has anti-cancer effects.

Product Other Information

Product Overview 5-Chloro-2-benzothiazolinone (CBT) is a chemical compound that has been studied for its potential applications in a variety of scientific research fields. CBT is a member of the benzothiazolinone family, which is a group of compounds used in the synthesis of other compounds and as a preservative. CBT has been studied for its potential as an antimicrobial agent, as well as its potential applications in the synthesis of other compounds.
Synthesis and Application 5-Chloro-2-benzothiazolinone is synthesized through a chemical process known as a Grignard reaction. This reaction involves the combination of a Grignard reagent, such as magnesium chloride, with an aldehyde or ketone. The reaction yields a benzothiazolinone product, which can then be further reacted with a chlorine source to yield 5-Chloro-2-benzothiazolinone. 5-Chloro-2-benzothiazolinone has been studied for its potential applications in a variety of scientific research fields. It has been studied as an antimicrobial agent, as a preservative, and as a potential component in the synthesis of other compounds. 5-Chloro-2-benzothiazolinone has also been studied for its potential applications in the fields of biochemistry, pharmacology, and immunology.
Future Directions There are a number of potential future directions for 5-Chloro-2-benzothiazolinone research. One potential direction is the development of new methods for synthesizing 5-Chloro-2-benzothiazolinone. Additionally, further research could be conducted into the effects of 5-Chloro-2-benzothiazolinone on various biochemical and physiological processes, as well as its potential applications in the synthesis of other compounds. Finally, further research could be conducted into the potential therapeutic applications of 5-Chloro-2-benzothiazolinone, such as its potential use as an antimicrobial agent or preservative.