4,4'-Biphenyldisulfonyl Chloride TCI B1165

Chemical Identity

CAS No.: 3406-84-6
PubChem: CID 76950·SID 87564105
Formula: C12H8Cl2O4S2
Molecular weight: 351.2 g/mol
Purity: >97.0%(T)(qNMR)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-(4-chlorosulfonylphenyl)benzenesulfonyl chloride
SMILES: C1=CC(=CC=C1C2=CC=C(C=C2)S(=O)(=O)Cl)S(=O)(=O)Cl
InChIKey: OTFAWEIFBPUXOH-UHFFFAOYSA-N

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4,4'-Biphenyldisulfonyl Chloride is a chemical compound widely used as a building block in the synthesis of complex organic molecules. It plays a crucial role in laboratory settings where researchers aim to construct larger molecular structures through various chemical reactions. This compound is particularly valuable in the field of organic chemistry due to its unique molecular structure, which consists of two phenyl rings connected by two sulfonate chloride groups. Its versatility makes it an essential tool for chemists working on the development of new compounds and materials.

The compound's stability and controlled reactivity make it a preferred choice for a variety of chemical reactions. Its ability to participate in nucleophilic reactions, substitution reactions, and coupling reactions ensures high efficiency and consistent results. The chemical properties of 4,4'-Biphenyldisulfonyl Chloride allow it to be used in applications requiring precision and reliability. This makes it an ideal component for research in both academic and industrial laboratories.

In Indonesian laboratories, 4,4'-Biphenyldisulfonyl Chloride is commonly used in organic chemistry research. It is a key reagent in the synthesis of heterocyclic compounds and other complex organic structures. Its availability and chemical properties make it a popular choice among researchers looking to advance their work in chemical synthesis and material development.

TCI brochures (PDF)

Monomers 2025-05-28 · p. 38

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Organic synthesis applications benefit from its role in constructing complex molecular frameworks through various reaction mechanisms.
It is ideal for nucleophilic substitution reactions due to its reactivity and stability under controlled conditions.
Coupling reactions often utilize this compound to link different molecular components efficiently.
Its use in heterocyclic compound synthesis supports the development of pharmaceutical and industrial materials.
It is a preferred reagent in research settings where precision and reproducibility are essential.

Brand	TCI
CAS number	3406-84-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid
Storage	Store in a cool, dry place away from moisture and direct sunlight

4,4'-Biphenyldisulfonyl Chloride should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent exposure to moisture and air. Due to its reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Storage should be in a location that is inaccessible to children and away from incompatible materials. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for laboratory use.

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