CAS 338453-16-0

cyclobutanesulfonyl chloride

Description:

Cyclobutanesulfonyl chloride is an organic compound characterized by the presence of a cyclobutane ring and a sulfonyl chloride functional group. It typically appears as a colorless to pale yellow liquid and is known for its reactivity, particularly due to the sulfonyl chloride moiety, which can act as a potent electrophile. This compound is often used in organic synthesis as a sulfonylating agent, facilitating the introduction of sulfonyl groups into various substrates. Its reactivity allows it to participate in nucleophilic substitution reactions, making it valuable in the preparation of sulfonamides and other derivatives. Cyclobutanesulfonyl chloride is sensitive to moisture and should be handled with care, as it can release hydrochloric acid upon hydrolysis. Additionally, it is important to consider safety precautions when working with this compound, as it can be corrosive and irritating to the skin and respiratory system. Overall, cyclobutanesulfonyl chloride is a useful reagent in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals.

Formula: C₄H₇ClO₂S

cyclobutanesulfonyl chloride

CAS: 338453-16-0

Formula: C₄H₇ClO₂S

Purity: 95%

Color and Shape: Liquid

Molecular weight: 154.6152

Ref: IN-DA00382Q

Cyclobutanesulfonyl chloride

CAS: 338453-16-0

Cyclobutanesulfonyl chloride

Purity: 95%

Color and Shape: Solid

Molecular weight: 154.62g/mol

Ref: 54-OR931640

Cyclobutanesulfonyl chloride

CAS: 338453-16-0

Formula: C₄H₇ClO₂S

Purity: 90%

Color and Shape: Solid

Molecular weight: 154.61

Ref: 10-F235870

Cyclobutanesulfonyl chloride

CAS: 338453-16-0

Cyclobutanesulfonyl chloride is a reagent that is used for the synthesis of 1-6-alkylcyclobutanes. It can be used to synthesize heterocyclic compounds, including those with high optical purity. Cyclobutanesulfonyl chloride has been shown to have antiviral and antiproliferative properties. It has also been shown to exhibit anticancer activity in vitro and in vivo. The mechanism of action for this compound is unclear, but it may inhibit protein synthesis by attacking the amino acid methionine in proteins or by inhibiting DNA replication.

Formula: C₄H₇ClO₂S

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 154.62 g/mol

Ref: 3D-FC161212