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2-Chloro-5-nitrophenyl isothiocyanate functions as a reagent in chemical synthesis, specifically in the modification of organic compounds. Its mechanism of action involves the reaction of the isothiocyanate group with nucleophiles, such as amines or thiols, to form thiourea or dithiocarbamate derivatives. 2-Chloro-5-nitrophenyl isothiocyanate may be used to introduce the isothiocyanate functional group into various organic molecules, allowing for the synthesis of diverse compounds with altered properties. The isothiocyanate group reacts with nucleophilic functional groups in the target molecules, leading to the formation of new covalent bonds. This reactivity enables the modification of organic compounds for the purpose of creating new materials or studying structure-activity relationships. In this way, 2-Chloro-5-nitrophenyl isothiocyanate plays a specific role in the functionalization of organic molecules within experimental applications, facilitating the synthesis of novel compounds for research and development purposes.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-Chloro-5-nitrophenyl isothiocyanate, 1 g | sc-281658 | 1 g | $35.00 |