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Methyl carbamate, 99%, Thermo Scientific Chemicals
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Catalog number A16523.18
also known as A16523-18
Price (USD)/ Each
24.00
-
Quantity:
50 g
Price (USD)/ Each
24.00
Methyl carbamate, 99%, Thermo Scientific Chemicals
Catalog numberA16523.18
Price (USD)/ Each
24.00
-
Chemical Identifiers
CAS598-55-0
Specifications
Specification Sheet
Specification SheetAppearance (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.
WARNING: Cancer – www.P65Warnings.ca.gov
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).