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Catalog Number:
23250
CAS Number:
1623-93-4
Chlorure de 4-biphénylsulfonyle
Purity:
≥ 97 % (dosage)
Synonym(s):
Chlorure de 1,1'-biphényl-4-sulfonyle
Hazmat
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Product Information

4-Biphenylsulfonyl chloride is a versatile reagent widely utilized in organic synthesis and pharmaceutical development. This compound serves as an effective sulfonylating agent, facilitating the introduction of sulfonyl groups into various organic molecules. Its unique structure allows for selective reactions, making it particularly valuable in the synthesis of sulfonamides and other biologically active compounds. Researchers appreciate its ability to enhance the solubility and stability of target molecules, which is crucial in drug formulation and development.

In addition to its applications in medicinal chemistry, 4-Biphenylsulfonyl chloride is also employed in the production of advanced materials and agrochemicals. Its reactivity and specificity make it an essential tool for chemists looking to create complex molecular architectures. The compound's efficiency in facilitating reactions can lead to reduced reaction times and improved yields, making it a preferred choice for both academic and industrial laboratories.

Synonyms
Chlorure de 1,1'-biphényl-4-sulfonyle
CAS Number
1623-93-4
Purity
≥ 97 % (dosage)
Molecular Formula
C12H9ClO2S
Molecular Weight
252.72
MDL Number
MFCD00078658
PubChem ID
74192
Melting Point
111 - 119 °C (lit.)
Appearance
Poudre/solide cristallin blanc
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Chlorure de 1,1'-biphényl-4-sulfonyle
CAS Number
1623-93-4
Purity
≥ 97 % (dosage)
Molecular Formula
C12H9ClO2S
Molecular Weight
252.72
MDL Number
MFCD00078658
PubChem ID
74192
Melting Point
111 - 119 °C (lit.)
Appearance
Poudre/solide cristallin blanc
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Biphenylsulfonyl chloride is widely utilized in research focused on:

  • Synthetic Chemistry: It serves as a key reagent in the synthesis of sulfonamide compounds, which are important in pharmaceuticals and agrochemicals.
  • Pharmaceutical Development: This compound is used to create various active pharmaceutical ingredients (APIs), enhancing drug efficacy and stability.
  • Polymer Chemistry: It acts as a coupling agent in the production of specialty polymers, improving their mechanical properties and thermal stability.
  • Analytical Chemistry: It is employed in the derivatization of amines and alcohols for better detection and quantification in chromatographic analyses.
  • Material Science: The compound is used in the development of advanced materials, such as coatings and adhesives, due to its excellent reactivity and functionalization capabilities.

Citations