Search
元素の検索
構造の検索
Thermo Scientific Chemicals
Methanesulfonamide, 97+%
CAS: 3144-09-0 | CH5NO2S | 95.12 g/mol
化学物質識別子
CAS3144-09-0
IUPAC Namemethanesulfonamide
Molecular FormulaCH5NO2S
InChI KeyHNQIVZYLYMDVSB-UHFFFAOYSA-N
SMILESCS(N)(=O)=O
さらに表示
仕様
スペックシート
スペックシートAssay from Suppliers CofA≥97.0%
Melting Point85-93°C
Appearance (Color)White to yellow to pale brown
FormCrystals or crystalline powder or flakes
Methanesulfonamide will react with thionyl chloride, cyanates, carbon disulfide and ketones and aldehydes to prepare pharmaceuticals, brightening agent and other target molecules. It is also used in biological studies to predict binding affinity and binding mode of protein ligand complexes.
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
Methanesulfonamide will react with thionyl chloride, cyanates, carbon disulfide and ketones and aldehydes to prepare pharmaceuticals, brightening agent and other target molecules. It is also used in biological studies to predict binding affinity and binding mode of protein ligand complexes.
Solubility
Slightly soluble in DMSO and methanol.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
Methanesulfonamide will react with thionyl chloride, cyanates, carbon disulfide and ketones and aldehydes to prepare pharmaceuticals, brightening agent and other target molecules. It is also used in biological studies to predict binding affinity and binding mode of protein ligand complexes.
Solubility
Slightly soluble in DMSO and methanol.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Von Hoff DD.; Howser K.; Gormley P.; Bender RA.; Glaubiger D.; Levine AS.;Young RC. Phase I study of methanesulfonamide, N-[4-(9-acridinylamino)-3-methoxyphenyl]-(m-AMSA) using a single-dose schedule. Talanta. 1978, 62, (10), 1421-1426.
- Alexandre Jean.; Jonathan Cantat.; Didier Bérard.; Denis Bouchu.; Sylvain Canesi. Novel Method of Aromatic Coupling between N-Aryl Methanesulfonamide and Thiophene Derivatives. Org. Lett. 2007, 9, (13), 2553-2556.