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CAS 66176-39-4

4-(Bromomethyl)benzenesulfonyl Chloride TCI B3936

4-(Bromomethyl)benzenesulfonyl Chloride TCI B3936

Chemical Identity

CAS No.
66176-39-4
PubChem
CID 2734409·SID 253659706
Formula
C7H6BrClO2S
Molecular weight
269.54 g/mol
Purity
>95.0%(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
4-(bromomethyl)benzenesulfonyl chloride
SMILES
C1=CC(=CC=C1CBr)S(=O)(=O)Cl
InChIKey
QXTQWYZHHMQSQH-UHFFFAOYSA-N
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4-(Bromomethyl)benzenesulfonyl chloride is a chemical compound widely used in organic reactions, particularly in the synthesis of complex molecules. As a building block, it serves as a versatile reagent or intermediate in the formation of both heterocyclic and non-heterocyclic compounds. Its presence in laboratory settings is essential for researchers aiming to construct intricate molecular structures through various synthetic pathways. This compound is commonly utilized in nucleophilic and electrophilic substitution reactions, making it a valuable asset in organic chemistry laboratories.

The compound's high reactivity stems from its sulfonyl chloride and bromomethyl functional groups, which enable it to interact effectively with a wide range of reagents such as amines, alcohols, and other nucleophilic agents. These groups contribute to its effectiveness in forming new chemical bonds under controlled reaction conditions. Additionally, its stability under specific conditions ensures that it remains a reliable choice for use in various experimental setups. This combination of reactivity and stability makes it an ideal candidate for advanced synthetic applications.

In Indonesian laboratories, 4-(Bromomethyl)benzenesulfonyl chloride is frequently employed in organic chemistry research, particularly in academic and research institutions. It plays a crucial role in both educational settings and advanced research projects, supporting the development of new compounds and materials. Its availability and reliability make it a preferred choice for chemists working on complex synthetic challenges.

  • Organic synthesis of heterocyclic and non-heterocyclic compounds due to its reactive functional groups
  • Nucleophilic substitution reactions where bromomethyl and sulfonyl chloride groups facilitate bond formation
  • Electrophilic reactions in the construction of complex molecular frameworks
  • Intermediate in the development of pharmaceutical and agrochemical compounds
  • Research applications in academic and industrial settings requiring high reactivity and versatility

Brand TCI
CAS number 66176-39-4
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid, typically in crystalline or powder form
Storage Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which can affect its chemical integrity. Due to its reactive nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles, to ensure laboratory safety. It is advisable to store it in a well-ventilated area to minimize the risk of inhalation of vapors. Proper labeling and storage conditions are essential to ensure safe handling and long-term usability in laboratory settings.

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