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CAS 27344-41-8

Disodium 4,4'-Bis(2-sulfonatostyryl)biphenyl TCI D3251

Disodium 4,4'-Bis(2-sulfonatostyryl)biphenyl TCI D3251

Chemical Identity

Other names
4,4'-Bis(2-sulfonatostyryl)biphenyl Disodium Salt
CAS No.
27344-41-8
PubChem
CID 5332133·SID 87558142
Formula
C28H20Na2O6S2
Molecular weight
562.56 g/mol
Purity
>97.0%(HPLC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
disodium;2-[(E)-2-[4-[4-[(E)-2-(2-sulfonatophenyl)ethenyl]phenyl]phenyl]ethenyl]benzenesulfonate
SMILES
C1=CC=C(C(=C1)C=CC2=CC=C(C=C2)C3=CC=C(C=C3)C=CC4=CC=CC=C4S(=O)(=O)[O-])S(=O)(=O)[O-].[Na+].[Na+]
InChIKey
PMPJQLCPEQFEJW-HPKCLRQXSA-L
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Disodium 4,4'-Bis(2-sulfonatostyryl)biphenyl is a chemical compound widely used in laboratory settings for the synthesis of complex organic molecules. As a building block in organic chemistry, it serves as a versatile intermediate that can undergo various chemical reactions, such as substitution or coupling reactions, to form more complex structures. This compound is particularly valuable in the development of materials with specific functional groups, due to its unique molecular architecture. Its presence in the laboratory enables chemists to explore new synthetic pathways and design compounds with tailored properties.

The compound's key characteristics include the presence of sulfonate groups, which enhance its solubility in aqueous solutions and contribute to its reactivity. The biphenyl core provides structural stability and allows for the attachment of diverse functional groups, making it a flexible starting material. These properties make it a preferred choice for researchers aiming to create compounds with specific optical, electronic, or chemical properties. Its reactivity and compatibility with a wide range of synthetic methods further support its use in both academic and industrial research.

In Indonesian laboratories, this compound is commonly used in organic synthesis and materials science research. It is a staple in chemical and pharmaceutical laboratories, where it is employed in the development of new compounds and the study of molecular interactions. Its role in the creation of complex structures makes it essential for both fundamental and applied research in the chemical sciences.

  • Organic Synthesis: This compound is ideal for creating complex organic molecules due to its reactivity and structural versatility.
  • Materials Science Research: Its biphenyl structure and sulfonate groups make it suitable for developing new materials with specific functional properties.
  • Pharmaceutical Development: It is used in the synthesis of compounds that may have therapeutic applications, supporting drug discovery efforts.
  • Chemical Education: It serves as a valuable teaching tool for students learning about organic reactions and molecular design.
  • Industrial Chemistry: It is applied in the production of specialty chemicals that require precise molecular structures and functional groups.

Brand TCI
CAS number 27344-41-8
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 (exact form may vary depending on supplier)
Storage Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers made of materials such as glass or polyethylene to prevent contamination and degradation. As a reactive chemical, it should be handled with appropriate personal protective equipment, including gloves and safety goggles, to ensure laboratory safety. Proper ventilation should be maintained when working with this compound to minimize exposure. It is important to keep it away from incompatible substances to prevent any potential chemical reactions. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in laboratory applications.

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