2,6-Difluorobenzenesulfonyl Chloride TCI D2940

Chemical Identity

CAS No.: 60230-36-6
PubChem: CID 2734271·SID 87569302
Formula: C6H3ClF2O2S
Molecular weight: 212.59 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2,6-difluorobenzenesulfonyl chloride
SMILES: C1=CC(=C(C(=C1)F)S(=O)(=O)Cl)F
InChIKey: QXWAUQMMMIMLTO-UHFFFAOYSA-N
MDL: MDL00085004

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2,6-Difluorobenzenesulfonyl Chloride is a chemical compound widely used as a building block in the synthesis of complex organic molecules. It is a key reagent in various organic reactions due to its unique molecular structure, which includes a sulfonate chloride group attached to a benzene ring with two fluorine atoms. This compound plays a vital role in modern laboratory settings, particularly in research involving functional group transformations and molecular modifications. Its versatility makes it an essential tool for chemists working on drug development and material science projects.

The compound is valued for its high reactivity and ability to form stable bonds with a wide range of functional groups. These properties make it an ideal choice for reactions requiring both stability and reactivity. Its chemical stability under controlled conditions further enhances its usability in laboratory environments. The combination of these characteristics allows researchers to achieve precise and efficient chemical transformations, contributing to the success of numerous scientific investigations.

In Indonesian laboratories, 2,6-Difluorobenzenesulfonyl Chloride is commonly used in organic chemistry and pharmacology research. Scientists rely on this compound to develop new compounds with potential medical or industrial applications. Its role in synthesizing bioactive molecules and functional materials underscores its importance in both academic and applied research settings across the country.

TCI brochures (PDF)

Fluorination Reagents, Fluorinated Building Blocks 2026-03-18 · p. 30

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Organic synthesis reactions benefit from this compound's reactivity and ability to form sulfonamide bonds, making it ideal for coupling reactions.
Drug development projects utilize its structural versatility to create novel pharmaceutical compounds with targeted biological activities.
Functional group modification experiments leverage its sulfonate chloride group for precise molecular alterations and substitutions.
Material science research employs it to synthesize advanced polymers and coatings with enhanced chemical resistance.
Analytical chemistry applications use it as a reagent for derivatization and spectroscopic analysis of complex organic compounds.

Brand	TCI
CAS number	60230-36-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid, crystalline
Storage	Store in a cool, dry place away from moisture and light

This compound should be stored in a cool, dry environment, away from moisture and direct light to maintain its chemical stability. It is recommended to use airtight containers made of materials such as glass or high-density polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation and avoid exposure to incompatible substances. Careful handling and controlled storage conditions are essential to preserve its effectiveness and ensure safe usage in research applications.

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