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Catalog Number:
23380
CAS Number:
885267-95-8
Chlorure de 3',5'-dichloro[1,1'-biphényl]-4-sulfonyle
Synonym(s):
Chlorure de 4-(3,5-dichlorophényl)benzènesulfonyle
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$249.07 /250 mg
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Product Information

3',5'-Dichloro[1,1'-biphenyl]-4-sulfonyl chloride is a versatile sulfonyl chloride compound known for its significant role in organic synthesis and pharmaceutical applications. This compound features a unique dichlorophenyl group, which enhances its reactivity and makes it an excellent intermediate for the synthesis of various biologically active molecules. Its sulfonyl chloride functionality allows for the introduction of sulfonyl groups into target compounds, facilitating the development of novel pharmaceuticals, agrochemicals, and fine chemicals. Researchers and industry professionals can leverage this compound to create potent inhibitors, dyes, and other specialty chemicals, making it a valuable addition to any synthetic chemistry toolkit.

The compound's ability to undergo nucleophilic substitution reactions opens up pathways for the development of complex molecular architectures. Its stability and reactivity make it particularly useful in the synthesis of sulfonamides and other derivatives, which are crucial in medicinal chemistry. With its broad applicability and unique properties, 3',5'-Dichloro[1,1'-biphenyl]-4-sulfonyl chloride stands out as a key building block for innovative research and product development.

Synonyms
Chlorure de 4-(3,5-dichlorophényl)benzènesulfonyle
CAS Number
885267-95-8
Molecular Formula
C12H7Cl3O2S
Molecular Weight
321.61
MDL Number
MFCD01631919
PubChem ID
3771398
Conditions
Conserver à 0-8°C
General Information
Synonyms
Chlorure de 4-(3,5-dichlorophényl)benzènesulfonyle
CAS Number
885267-95-8
Molecular Formula
C12H7Cl3O2S
Molecular Weight
321.61
MDL Number
MFCD01631919
PubChem ID
3771398
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3',5'-Dichloro[1,1'-biphenyl]-4-sulfonyl chloride is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and anti-cancer agents.
  • Organic Synthesis: It is employed in organic chemistry for the preparation of sulfonamide derivatives, which are crucial in creating a range of biologically active compounds.
  • Agricultural Chemicals: The compound is used in the formulation of agrochemicals, enhancing the effectiveness of pesticides and herbicides by improving their stability and solubility.
  • Material Science: It plays a role in the production of specialty polymers and resins, contributing to materials with enhanced thermal and chemical resistance.
  • Analytical Chemistry: This chemical is utilized in the development of analytical methods for detecting and quantifying various substances, aiding in quality control processes in laboratories.

Citations