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Atomfair 2-Cyanoethyl methyl carbonate C5H7NO3

Description 2-Cyanoethyl Methyl Carbonate (CAS No. 260362-83-2) is a high-purity specialty chemical with the molecular formula C5H7NO3. This organic carbonate derivative is characterized by its cyanoethyl functional group, which enhances reactivity and solubility in polar solvents. It is synthesized under stringent conditions to ensure >98% purity, as verified by GC-MS and NMR analysis. Ideal for advanced research applications, this compound is supplied in amber glass bottles under inert gas to prevent degradation. Researchers value its stability and versatility in organic synthesis, particularly in the development of novel electrolytes, polymer precursors, and pharmaceutical intermediates. Store in a cool, dry place away…

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Description

Description

2-Cyanoethyl Methyl Carbonate (CAS No. 260362-83-2) is a high-purity specialty chemical with the molecular formula C5H7NO3. This organic carbonate derivative is characterized by its cyanoethyl functional group, which enhances reactivity and solubility in polar solvents. It is synthesized under stringent conditions to ensure >98% purity, as verified by GC-MS and NMR analysis. Ideal for advanced research applications, this compound is supplied in amber glass bottles under inert gas to prevent degradation. Researchers value its stability and versatility in organic synthesis, particularly in the development of novel electrolytes, polymer precursors, and pharmaceutical intermediates. Store in a cool, dry place away from moisture and strong oxidizers.

  • CAS No: 260362-83-2
  • Molecular Formula: C5H7NO3
  • Molecular Weight: 129.11
  • Exact Mass: 129.042593085
  • Monoisotopic Mass: 129.042593085
  • IUPAC Name: 2-cyanoethyl methyl carbonate
  • SMILES: COC(=O)OCCC#N

Application

2-Cyanoethyl Methyl Carbonate is widely used as a reactive intermediate in organic synthesis, particularly in the preparation of carbonate-based electrolytes for lithium-ion batteries. Its cyanoethyl group enables selective modifications in polymer chemistry, making it valuable for creating tailored macromolecules. Researchers also employ it as a protecting group for alcohols and diols in multistep synthetic routes.

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