acetyl Methanesulfonate
acetyl Methanesulfonate Basic information
- Product Name:
- acetyl Methanesulfonate
- Synonyms:
-
- acetyl Methanesulfonate
- Methanesulfonyl acetate
- NSC 158252
- Busulfan Impurity 6
- Acetic acid, anhydride with methanesulfonic acid
- Busulfan Impurity 10
- CAS:
- 5539-53-7
- MF:
- C3H6O4S
- MW:
- 138.14
- Mol File:
- 5539-53-7.mol
acetyl Methanesulfonate Chemical Properties
- Boiling point:
- 56 °C(Press: 0.01 Torr)
- Density
- 1.346±0.06 g/cm3(Predicted)
- storage temp.
- Hygroscopic, Refrigerator, under inert atmosphere
- solubility
- Chloroform (Sparingly)
- form
- Oil
- color
- Yellow
- Stability:
- Extremely Moisture Sensitive
acetyl Methanesulfonate Usage And Synthesis
Uses
Acetyl Methanesulfonate, is an impurity of Busulfan (B689900), an alkylating agent with antileukemic activity. Antineoplastic. It is a reagent for ether cleavage, for the cleavage of activated cyclopropanes as partial structures of cyclopropyl ketones, and for acetylation of aromatic rings.
Preparation
Preparative Methods: Acetyl Methanesulfonate can be prepared on a large scale (1 mol) from Acetyl Chloride and Methanesulfonic Acid by heating at reflux followed by fractional distillation (85% yield).
storage
Handling, Storage, and Precautions: slightly hygroscopic. However, no particular precautions are required upon exposure to air for a short period of time. acetyl Methanesulfonate is stable if stored at 4 °C for several months. Use in a fume hood.
Purification Methods
The main impurity is methanesulfonic acid. Reflux it with redistilled acetyl chloride for 6-10hours, i.e. until no further HCl is absorbed in a trap, and exclude moisture. Distil off excess of AcCl and carefully distil it below 0.001mm with the bath temperature below 120o to give the anhydride as a pale yellow oil which solidifies below 0o. Below ~130o it gives the disulfonic anhydride, and above ~130o polymers are formed, and it is used for cleaving ethers [Preparation, IR, NMR: Karger & Mazur J Org Chem 36 528, 532 1971]. [Beilstein 2 H 166, 2 III 349.]
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