Benzylsulfonyl Chloride TCI B0441

Chemical Identity

CAS No.: 1939-99-7
PubChem: CID 74740·SID 87563478
Formula: C7H7ClO2S
Molecular weight: 190.65 g/mol
Purity: >97.0%(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: phenylmethanesulfonyl chloride
SMILES: C1=CC=C(C=C1)CS(=O)(=O)Cl
InChIKey: OAHKWDDSKCRNFE-UHFFFAOYSA-N

Rp 1.618.050,00

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Benzylsulfonyl Chloride (BCS) is a chemical compound widely used as a building block in organic synthesis. It plays a crucial role in laboratory settings by enabling the formation of sulfonate linkages through various chemical reactions. This compound is particularly valuable in nucleophilic substitution and molecular coupling reactions, where its reactivity and structural versatility make it an essential tool for chemists. Its presence in the synthesis of complex organic molecules supports research in pharmaceuticals, materials science, and industrial chemistry.

The chemical properties of BCS make it a preferred choice for laboratory use. Its molecular structure contains a chloride group, which enhances its reactivity towards a wide range of reagents. The compound exhibits good solubility in organic solvents, facilitating easy mixing and reaction processes. Additionally, BCS is chemically stable under controlled conditions, though it remains highly reactive to water and bases. These characteristics ensure its effectiveness in various synthetic pathways, making it a reliable reagent for organic chemists.

In Indonesian laboratories, BCS is extensively used in organic chemistry research. It is commonly found in the synthesis of pharmaceutical compounds and industrial chemicals. Its role in creating complex molecular structures is vital for developing new drug candidates and advanced materials. The compound’s availability and performance make it a staple in both academic and industrial research environments across Indonesia.

Related TCI products

Organic synthesis for creating sulfonate linkages due to its reactivity and structural versatility.
Nucleophilic substitution reactions where its chloride group facilitates efficient substitution processes.
Molecular coupling reactions to form complex organic compounds with high specificity.
Pharmaceutical research for the development of new drug molecules and bioactive compounds.
Industrial chemical production for the synthesis of specialty chemicals and polymers.

Brand	TCI
CAS number	1939-99-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Liquid
Storage	Store in a cool, dry place away from moisture and bases

Benzylsulfonyl Chloride should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity with water and bases, it should be handled in a fume hood to ensure safety. Suitable containers for storage include glass or high-density polyethylene vessels. Always use appropriate personal protective equipment when handling this compound. Regular monitoring of storage conditions is essential to maintain its integrity and effectiveness in laboratory applications.

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