CAS 812-01-1
:Chlorosulfuric acid, methyl ester
Description:
Chlorosulfuric acid, methyl ester, also known as methyl chlorosulfate, is an organosulfur compound characterized by its reactive nature and utility in organic synthesis. It is a colorless to pale yellow liquid with a pungent odor, and it is highly corrosive and toxic. The compound features a chlorosulfate functional group, which imparts significant reactivity, particularly in nucleophilic substitution reactions. It is soluble in organic solvents but reacts vigorously with water, releasing hydrochloric acid and sulfuric acid, which can pose safety hazards. Methyl chlorosulfate is primarily used as a reagent in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. Due to its corrosive properties, it requires careful handling and storage in appropriate materials to prevent degradation and ensure safety. Additionally, it is important to note that exposure to this compound can lead to severe health effects, necessitating the use of personal protective equipment during its manipulation.
Formula:CH3ClO3S
InChI:InChI=1S/CH3ClO3S/c1-5-6(2,3)4/h1H3
InChI key:InChIKey=KNVLCWQKYHCADB-UHFFFAOYSA-N
SMILES:S(OC)(Cl)(=O)=O
Synonyms:- Chlorosulfonic acid, methyl ester
- Chlorosulfuric acid, methyl ester
- Methyl Sulfurochloridate
- Methyl chlorosulfate
- Methyl chlorosulfonate
- [(Chlorosulfonyl)oxy]methane
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Found 5 products.
Chlorosulfuric acid, methyl ester
CAS:Formula:CH3ClO3SPurity:98%Color and Shape:LiquidMolecular weight:130.5507Chlorosulfuric Acid Methyl Ester
CAS:Controlled ProductStability Moisture Sensitive
Applications Chlorosulfuric Acid Methyl Ester is used in the synthesis of acetylenic TACE inhibitors in the treatment of arthritis.
E0
References Levin, J. et al.: Bioorg. Med. Chem. Lett., 15, 4345 (2005);Formula:CH3ClO3SColor and Shape:NeatMolecular weight:130.55
