Nom du produit:5-Chloro-2-benzothiazolinone

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

CAS:20600-44-6
Formule moléculaire:C7H4ClNOS
Pureté:95%+
Numéro de catalogue:CM156973
Poids moléculaire:185.63

Unité d'emballage Stock disponible Prix($) Quantité
CM156973-25g in stock ƴœ
CM156973-100g in stock džŸƚ

Pour une utilisation en R&D uniquement..

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Détails du produit

N° CAS:20600-44-6
Formule moléculaire:C7H4ClNOS
Point de fusion:-
Code SMILES:O=C1SC2=CC=C(Cl)C=C2N1
Densité:
Numéro de catalogue:CM156973
Poids moléculaire:185.63
Point d'ébullition:
N° Mdl:MFCD00060125
Stockage: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.