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CAS 54322-31-5

4-(2-Bromoethyl)benzenesulfonic Acid TCI B2006

4-(2-Bromoethyl)benzenesulfonic Acid TCI B2006

Chemical Identity

CAS No.
54322-31-5
PubChem
CID 103071·SID 87564886
Formula
C8H9BrO3S
Molecular weight
265.13 g/mol
Purity
>97.0%(T)(HPLC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
4-(2-bromoethyl)benzenesulfonic acid
SMILES
C1=CC(=CC=C1CCBr)S(=O)(=O)O
InChIKey
XRPCDXSRXPQUKT-UHFFFAOYSA-N
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4-(2-Bromoethyl)benzenesulfonic Acid is a chemical compound widely used in organic synthesis reactions. It serves as a key building block in the development of complex chemical structures, playing a crucial role in laboratory settings where synthetic chemistry is practiced. This compound is commonly found in chemical laboratories as a foundational material for creating a variety of synthetic compounds. Its versatility makes it an essential component in the toolkit of chemists working on diverse research projects.

The compound's reactivity is largely attributed to the presence of both bromo and sulfonate functional groups, which contribute to its high reactivity. These groups enable it to participate in substitution and electrophilic reactions, making it highly valuable in the synthesis of both heterocyclic and non-heterocyclic compounds. Its chemical structure allows for a wide range of chemical transformations, which is why it is frequently used in advanced synthetic pathways.

In Indonesian laboratories, this compound is particularly relevant for organic chemistry research, especially in academic and research institutions. It is often utilized in projects focused on the synthesis of pharmacological compounds and other specialized chemical materials. Its stability under certain conditions also makes it suitable for use in various research scales, from small-scale experiments to larger, more complex studies.

  • Organic synthesis projects benefit from this compound due to its reactivity and ability to form diverse chemical structures.
  • It is ideal for electrophilic substitution reactions because of its sulfonate group, which enhances reactivity in synthetic pathways.
  • In pharmaceutical research, it is used to develop new drug compounds by participating in key synthetic steps.
  • It supports the creation of heterocyclic compounds, which are essential in medicinal chemistry and material science.
  • Its stability and solubility properties make it suitable for use in both academic and industrial research settings.

Brand TCI
CAS number 54322-31-5
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per supplier offerings
Physical form Solid or liquid, depending on the specific formulation
Storage Store in a cool, dry place away from direct sunlight and incompatible materials

This compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air, which could affect its reactivity. Due to its chemical nature, it should be stored away from incompatible substances such as strong oxidizers or bases. Proper ventilation is essential when handling this material to minimize exposure risks. Laboratory personnel should always use appropriate personal protective equipment, including gloves and safety goggles, when working with this compound. Regular inspection of storage conditions is advised to ensure the material remains stable and safe for use.

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