Thiocyanic acid (2-benzothiazolylthio)methyl ester
Analytical Control
Reagent
Code: #52015
Alias
Benzothiazine; 2-(thiocyanate methylmercapto)benzothiazole, 2-(cyanothiomethylthio)benzothiazole, benzothiazine, thiocyanate (2-benzothiazolylthio)methanol (Base) ester, 2-thiocyanomethylthiobenzothiazole
CAS Number
21564-17-0
blur_circular Chemical Specifications
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Molecular Information
Weight
238.34 g/mol
Formula
C₉H₆N₂S₃
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Registry Numbers
EC Number
244-445-0
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Storage & Handling
Storage
2~8°C
description Product Description
Thiocyanic acid (2-benzothiazolylthio)methyl ester is primarily utilized in the field of organic synthesis and chemical research. It serves as a valuable intermediate in the preparation of various heterocyclic compounds, particularly those involving benzothiazole derivatives. These derivatives are often explored for their potential applications in pharmaceuticals, agrochemicals, and materials science. Additionally, this compound is studied for its role in the development of novel chemical reactions and catalytic processes, contributing to advancements in synthetic methodologies. Its unique structure makes it a useful reagent in the modification of organic molecules, enabling the creation of complex structures with specific functional properties.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Infrared Spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Appearance | white solid or red-brown liquid |
shopping_cart Available Sizes & Pricing
Thiocyanic acid (2-benzothiazolylthio)methyl ester
Thiocyanic acid (2-benzothiazolylthio)methyl ester is primarily utilized in the field of organic synthesis and chemical research. It serves as a valuable intermediate in the preparation of various heterocyclic compounds, particularly those involving benzothiazole derivatives. These derivatives are often explored for their potential applications in pharmaceuticals, agrochemicals, and materials science. Additionally, this compound is studied for its role in the development of novel chemical reactions and catalytic processes, contributing to advancements in synthetic methodologies. Its unique structure makes it a useful reagent in the modification of organic molecules, enabling the creation of complex structures with specific functional properties.
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