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Catalog Number:
23486
CAS Number:
885950-86-7
Cloruro de [3-(4-metilfenoxi)fenil]sulfonilo
Purity:
≥ 99 % (HPLC)
Synonym(s):
Cloruro de 3-(4-metilfenoxi)bencenosulfonilo
Documents
$201.60 /100 mg
Tamaño
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Product Information

[3-(4-Methylphenoxy)phenyl]sulfonyl chloride is a versatile sulfonyl chloride compound known for its utility in organic synthesis and pharmaceutical applications. This compound features a sulfonyl chloride functional group, which makes it an excellent reagent for the introduction of sulfonyl groups into various organic molecules. Its unique structure allows for the selective modification of aromatic compounds, facilitating the development of complex molecules in medicinal chemistry. Researchers and industry professionals can leverage this compound in the synthesis of sulfonamide drugs, agrochemicals, and other specialty chemicals, enhancing the efficiency of their chemical processes.

The compound's ability to act as a sulfonating agent provides significant advantages in the creation of sulfonyl derivatives, which are crucial in the development of biologically active compounds. It is particularly valuable in the pharmaceutical industry for the synthesis of sulfonamide antibiotics and other therapeutic agents. Additionally, its compatibility with various reaction conditions makes it a preferred choice for chemists looking to streamline their synthetic pathways. With its robust reactivity and application potential, [3-(4-Methylphenoxy)phenyl]sulfonyl chloride stands out as a key building block in modern organic chemistry.

Synonyms
Cloruro de 3-(4-metilfenoxi)bencenosulfonilo
CAS Number
885950-86-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C13H11ClO3S
Molecular Weight
282.75
MDL Number
MFCD02089489
PubChem ID
3840556
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Cloruro de 3-(4-metilfenoxi)bencenosulfonilo
CAS Number
885950-86-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C13H11ClO3S
Molecular Weight
282.75
MDL Number
MFCD02089489
PubChem ID
3840556
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

[3-(4-Methylphenoxy)phenyl]sulfonyl chloride is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in creating sulfonamide drugs that are effective against bacterial infections.
  • Agricultural Chemicals: It is used to develop agrochemicals, including herbicides and fungicides, which help improve crop yields and protect against pests, thus enhancing food security.
  • Polymer Chemistry: The compound acts as a coupling agent in polymer synthesis, allowing for the modification of polymer properties, which is essential in producing high-performance materials.
  • Research Reagents: It functions as a reagent in organic synthesis, facilitating the introduction of sulfonyl groups into various organic molecules, which is crucial for researchers in developing new compounds.
  • Diagnostic Agents: This chemical is explored for its potential in creating diagnostic agents that can improve the detection of diseases, contributing to advancements in medical diagnostics.

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