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N,N-Diisopropylcarbamoyl chloride functions as an acylating agent in various organic synthesis. Its mechanism of action involves the acylation of amines and alcohols, leading to the formation of amides and esters, respectively. N,N-Diisopropylcarbamoyl Chloride reacts with nucleophiles to form stable amide or ester linkages, making it useful in the modification of organic molecules. In experimental applications, N,N-Diisopropylcarbamoyl chloride is utilized to introduce the diisopropylcarbamoyl (DIPC) protecting group in peptide synthesis, allowing for the selective protection of amino groups. N,N-Diisopropylcarbamoyl Chloride′s mechanism of action involves the formation of stable amide bonds with the amino groups, preventing unwanted reactions during peptide assembly. N,N-Diisopropylcarbamoyl chloride is utilized in the preparation of various agrochemicals, where its acylating properties play a role in the synthesis of target compounds.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
N,N-Diisopropylcarbamoyl chloride, 5 g | sc-236118 | 5 g | $89.00 |