4-methylbenzothiazol-2-amine monohydrochloride

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What is the 4-methylbenzothiazol-2-amine monohydrochloride ?

4-methylbenzothiazol-2-amine monohydrochloride is , while it's Molecular Formula is C8H8 N2 S . Cl H. Used in Organic Synthesis:
4-methylbenzothiazol-2-amine monohydrochloride is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Industry:
As a building block for pharmaceuticals, 4-methylbenzothiazol-2-amine monohydrochloride is utilized in the development of new drugs, owing to its chemical properties that can be incorporated into medicinal compounds.
Used in Dye Industry:
4-methylbenzothiazol-2-amine monohydrochloride serves as a dye intermediate, playing a crucial role in the production of various dyes that have applications in different industries, including textiles and printing.
Used in Production of Fluorescent Whitening Agents:
4-methylbenzothiazol-2-amine monohydrochloride is employed in the creation of fluorescent whitening agents, which are used to enhance the brightness and whiteness of various products.
Used in Neuroscience Research:
In the field of neuroscience, 4-methylbenzothiazol-2-amine monohydrochloride is used as a fluorescent label for the visualization of neurons and other cells in biological tissues, aiding researchers in studying cellular structures and functions.

What is the CAS number for 4-methylbenzothiazol-2-amine monohydrochloride ?

The CAS number of 4-methylbenzothiazol-2-amine monohydrochloride is 64036-72-2.

More information of 4-methylbenzothiazol-2-amine monohydrochloride 64036-72-2 are:

What is 4-methylbenzothiazol-2-amine monohydrochloride (64036-72-2) used for?

4-methylbenzothiazol-2-amine monohydrochloride is a chemical compound with the molecular formula C8H9N2S·HCl, belonging to the benzothiazole family. It is a stable monohydrochloride salt form that exhibits improved water solubility compared to the free base form. 4-methylbenzothiazol-2-amine monohydrochloride is characterized by its potential as a reagent in organic synthesis and as a building block for pharmaceuticals, along with its applications as a dye intermediate and in the production of fluorescent whitening agents. Furthermore, it has been utilized in the field of neuroscience for the fluorescent labeling of neurons and other cells in biological tissues.

InChI:InChI=1/C8H8N2S.ClH/c1-5-3-2-4-6-7(5)10-8(9)11-6;/h2-4H,1H3,(H2,9,10);1H

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