109317-52-4

Basic information

• Product Name: 2-AMino-5,5-diMethyl-5,6-dihydro-4H-benzothiazol-7-one bydrobroMide
• Synonyms: 2-AMino-5,5-diMethyl-5,6-dihydro-4H-benzothiazol-7-one bydrobroMide;2-AMino-5,5-diMethyl-5,6-dihydrobenzo[d]thiazol-7(4H)-one hydrobroMide;2-Amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-one Hydrobromide
• CAS NO: 109317-52-4
• Molecular Formula: C9H13BrN2OS
• Molecular Weight: 277.18132
• Mol File: 109317-52-4.mol

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-AMino-5,5-diMethyl-5,6-dihydro-4H-benzothiazol-7-one bydrobroMide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMino-5,5-diMethyl-5,6-dihydro-4H-benzothiazol-7-one bydrobroMide(109317-52-4)
• EPA Substance Registry System: 2-AMino-5,5-diMethyl-5,6-dihydro-4H-benzothiazol-7-one bydrobroMide(109317-52-4)

Safety Data

• Hazardous Substances Data: 109317-52-4(Hazardous Substances Data)

Usage

Uses

Used in Agricultural Industry:
2-Amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-one hydrobromide is used as a fungicide for controlling fungal infections in crops. Its fungicidal activity helps protect plants from diseases and ensures a healthy and productive agricultural yield.
Used in Pharmaceutical Industry:
2-Amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-one hydrobromide is used as a building block in the synthesis of pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
2-Amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-one hydrobromide is used as a key intermediate in the synthesis of various organic compounds. Its versatile structure allows for the creation of a wide range of chemical products, including dyes, pigments, and other specialty chemicals.

Upstream product

• 1195-91-1 2-bromodimedone 
• 17356-08-0 thiourea 

Relevant articles and documents

Condensed Tetrahydrobenzothiazoles: Part IV - Synthesis of Some 2-Substituted 4,5,6,7-Tetrahydrobenzothiazoles and Their 5,5 Dimethyl-7-oxo Derivatives

Condensation of 2-chlorocyclohexanone (I) with substituted thioamides (II) in hot ethanol affords 2-substituted 4,5,6,7-tetrahydrobenzothiazoles (III).A similar reaction of 2-bromodimedone (IV) with II does not give 2-substituted 5,5-dimethyl-7-oxo-4,5,6,7-tetrahydrobenzothiazoles alone (V); a gummy product containing more than two compounds (TLC) is obtained in each case.However, When the reaction is carried out in THF at room temperature for 36 hr, the expected hydrobromide salts (Va) are obtained in excellent yields.The free bases (V) are liberated from Va by treatment with Na2CO3 solution.Structures of III, Va and V have been established by elemental analyses and spectral data.They do not exhibit any significant antifungal or antibacterial activity in vitro.