Isopropylsulfonyl Chloride TCI I0291

Chemical Identity

CAS No.: 10147-37-2
PubChem: CID 82408·SID 87571651
Formula: C3H7ClO2S
Molecular weight: 142.61 g/mol
Purity: >95.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: propane-2-sulfonyl chloride
SMILES: CC(C)S(=O)(=O)Cl
InChIKey: DRINJBFRTLBHNF-UHFFFAOYSA-N

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Isopropylsulfonyl Chloride (TCI I0291), with CAS number 10147-37-2, is a chemical compound widely used in organic laboratory reactions. It serves as a key building block in the synthesis of complex molecules, particularly in reactions involving sulfonation and substitution. Its chemical structure enables it to participate in various important reactions, making it a valuable reagent for chemists and researchers. This compound is commonly utilized in the development of heterocyclic compounds, pharmaceuticals, and industrial chemicals due to its reactivity and versatility.

Isopropylsulfonyl Chloride is known for its high reactivity, especially towards nucleophiles and bases. This reactivity makes it an ideal choice for reactions that require sulfonation or substitution mechanisms. Its ability to activate sulfonate groups allows it to be a crucial component in the synthesis of complex organic structures. Additionally, its chemical properties make it suitable for a wide range of synthetic applications, contributing to its popularity among laboratory professionals.

In Indonesian laboratories, Isopropylsulfonyl Chloride is frequently used by chemists and scientists in research and development projects. Its availability and effectiveness in various chemical reactions make it a preferred choice for those working on the synthesis of new compounds. The compound is particularly useful in applications requiring precise and controlled chemical transformations, supporting both academic and industrial research efforts.

Related TCI products

Synthesis of heterocyclic compounds requiring sulfonation reactions due to its ability to activate sulfonate groups.
Development of complex pharmaceuticals where sulfonate functionalities are essential for molecular structure.
Organic reactions involving substitution mechanisms where nucleophilic attack is required.
Industrial chemical synthesis processes that demand high reactivity and specificity in functional group modification.
Research applications in academic and industrial settings where controlled chemical transformations are necessary.

Brand	TCI
CAS number	10147-37-2
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	—
Physical form	—
Storage	Requires storage in a cool, dry place away from moisture and incompatible substances.

Isopropylsulfonyl Chloride should be stored in a cool, dry environment to maintain its chemical integrity. It is essential to keep the compound away from moisture and incompatible materials to prevent degradation or hazardous reactions. Suitable containers should be made of materials that resist chemical attack, such as glass or high-density polyethylene. Due to its corrosive and toxic nature, it must be handled with appropriate personal protective equipment. Laboratory personnel should ensure proper ventilation and follow established safety protocols to minimize exposure risks. Regular monitoring of storage conditions is recommended to ensure the compound remains stable and safe for use.

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