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Thermo Scientific Chemicals
Methyl carbamate, 99%
CAS: 598-55-0 | C2H5NO2 | 75.07 g/mol
化学物質識別子
CAS598-55-0
IUPAC Namemethyl carbamate
Molecular FormulaC2H5NO2
InChI KeyGTCAXTIRRLKXRU-UHFFFAOYSA-N
SMILESCOC(N)=O
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仕様
スペックシート
スペックシートAppearance (Color)White
Assay (GC)≥98.5%
Melting Point (clear melt)51-57°C
FormCrystals or crystalline powder
Identification (FTIR)Conforms
Methyl carbamate was used in the synthesis of protected aminocyclopropanes.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Methyl carbamate was used in the synthesis of protected aminocyclopropanes.
Solubility
Soluble in water(20g/L).
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, metals, alkali metals.
Methyl carbamate was used in the synthesis of protected aminocyclopropanes.
Solubility
Soluble in water(20g/L).
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, metals, alkali metals.
RUO – Research Use Only
General References:
- Qi-Feng Li,; Jun-Wei Wang,; Wen-Sheng Dong,; Mao-Qing Kang,; Xin-Kui Wang,; Shao-Yi Peng. A phosgene-free process for the synthesis of methyl N-phenyl carbamate by the reaction of aniline with methyl carbamate. Journal of Molecular Catalysis A: Chemical. 2004, 212 (1-2), 99-105.
- The Na derivative has been used as an ammonia equivalent in the Pd(0)-catalyzed amination of allylic acetates: Chem. Lett., 2123 (1989).