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Atomfair tert-Butyl isocyanoacetate C7H11NO2
Description tert-Butyl isocyanoacetate (CAS No. 2769-72-4) is a highly versatile organic compound with the molecular formula C7H11NO2. This colorless to pale yellow liquid is widely used in organic synthesis, particularly in the preparation of heterocycles, peptides, and other bioactive molecules. Its IUPAC name, tert-butyl 2-isocyanoacetate , reflects its functional groups: an isocyano moiety and a tert-butyl ester, which contribute to its reactivity and stability under various conditions. With a purity of ??95% (GC), this reagent is ideal for researchers in medicinal chemistry, catalysis, and materials science. It is packaged under inert gas to ensure stability and shipped with detailed technical…
Description
Description
tert-Butyl isocyanoacetate (CAS No. 2769-72-4) is a highly versatile organic compound with the molecular formula C7H11NO2. This colorless to pale yellow liquid is widely used in organic synthesis, particularly in the preparation of heterocycles, peptides, and other bioactive molecules. Its IUPAC name, tert-butyl 2-isocyanoacetate, reflects its functional groups: an isocyano moiety and a tert-butyl ester, which contribute to its reactivity and stability under various conditions.
With a purity of ??95% (GC), this reagent is ideal for researchers in medicinal chemistry, catalysis, and materials science. It is packaged under inert gas to ensure stability and shipped with detailed technical data, including NMR and MS spectra. Store in a cool, dry place away from moisture and strong oxidizers.
- CAS No: 2769-72-4
- Molecular Formula: C7H11NO2
- Molecular Weight: 141.17
- Exact Mass: 141.078978594
- Monoisotopic Mass: 141.078978594
- IUPAC Name: tert-butyl 2-isocyanoacetate
- SMILES: CC(C)(C)OC(=O)C[N+]#[C-]
- Synonyms: tert-Butyl isocyanoacetate, 2769-72-4, DTXSID70374780, DTXCID90325810, 628-840-9
Application
tert-Butyl isocyanoacetate is a key building block in multicomponent reactions (MCRs), such as the Ugi and Passerini reactions, enabling rapid synthesis of complex scaffolds. It is also employed in peptide modifications and as a precursor for agrochemicals and pharmaceuticals. Its isocyano group facilitates cycloadditions and nucleophilic additions, making it valuable for heterocycle formation.
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