CAS 53298-29-6

Carbonochloridic acid, 2-(methylsulfonyl)ethyl ester

Description:

Carbonochloridic acid, 2-(methylsulfonyl)ethyl ester, with the CAS number 53298-29-6, is an organic compound characterized by its ester functional group and the presence of a chlorocarbonyl moiety. This compound typically exhibits a polar nature due to the presence of the sulfonyl group, which can influence its solubility in various solvents. The methylsulfonyl group contributes to its reactivity, making it a potential intermediate in organic synthesis. The chlorocarbonyl group can participate in nucleophilic acyl substitution reactions, allowing for further functionalization. Additionally, the compound may exhibit moderate volatility and stability under standard conditions, but it should be handled with care due to the potential reactivity of the chlorinated functional groups. Its applications may include use in the synthesis of pharmaceuticals, agrochemicals, or other fine chemicals, where the unique properties of the methylsulfonyl group can be advantageous. As with many chemical substances, safety precautions should be observed when handling this compound due to potential toxicity and environmental impact.

Formula: C₄H₇ClO₄S

InChI: InChI=1/C4H7ClO4S/c1-10(7,8)3-2-9-4(5)6/h2-3H2,1H3

InChI key: InChIKey=KRGWSYPAFWHXQI-UHFFFAOYSA-N

SMILES: C(COC(Cl)=O)S(C)(=O)=O

Synonyms:

• 2-(Methylsulfonyl)Ethyl Carbonochloridate
• 2-(Methylsulfonyl)ethyl chloroformate
• 2-Methanesulfonylethyl chloroformate
• Carbonochloridic acid, 2-(methylsulfonyl)ethyl ester
• Methylsulfonylethoxycarbonyl chloride
• Methylsulfonylethyloxycarbonyl group
• 2-Mesylethyl chloroformate
• 2-METHYLSULFONYLETHYL CHLOROCARBONATE
• {2-[(chlorocarbonyl)oxy]ethanesulfonyl}methane
• Chloroformic acid 2-methylsulfonylethyl ester
• Einecs 258-463-1

{2-[(Chlorocarbonyl)oxy]ethanesulfonyl}methane

CAS: 53298-29-6

2-[(Chlorocarbonyl)oxy]ethanesulfonyl}methane (CESM) is an organic solvent that has been shown to initiate polymerization of vinyl monomers. It reacts with electrophiles such as hydroxyl groups and fluorine, and undergoes ligation reactions with reactive functional groups. CESM is also used as a reagent in chemical ligation reactions, which have been used for the synthesis of proteins with novel sequences. The use of CESM in these reactions has been shown to be more efficient than traditional methods, with the rate of reaction being increased by up to five times. This agent has also been shown to be effective against infectious diseases such as HIV-1 and other retroviruses. CESM deprotects nitro groups from peptides and proteins, enabling their cleavage by proteases or reduction by hydrogenation agents. The trifluoromethyl group on CESM can react with hydrocarbon groups

Formula: C₄H₇ClO₄S

Purity: Min. 95%

Molecular weight: 186.61 g/mol

Ref: 3D-DCA29829