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Catalog Number:
44312
CAS Number:
59337-92-7
Methyl 3-(chlorosulfonyl)-2-thiophenecarboxylate
Purity:
≥ 90% (GC)
Synonym(s):
2-Carbomethoxy-3-thiophenesulfonyl chloride, 3-(Chlorosulfonyl)-2-thiophenecarboxylic acid methyl ester, 2-(Methoxycarbonyl)-3-thiophenesulfonyl chloride
Hazmat
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$113.07 /5G
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Product Information

Methyl 3-(chlorosulfonyl)-2-thiophenecarboxylate is a versatile compound known for its unique sulfonyl functional group, which enhances its reactivity and application potential in various chemical processes. This compound is particularly valuable in the synthesis of agrochemicals and pharmaceuticals, where it serves as an intermediate in the production of biologically active molecules. Its ability to introduce a chlorosulfonyl group makes it an essential building block for creating sulfonamide derivatives, which are widely used in medicinal chemistry.

In addition to its applications in drug development, Methyl 3-(chlorosulfonyl)-2-thiophenecarboxylate is also utilized in materials science, particularly in the development of specialty polymers and coatings that require enhanced chemical resistance and stability. Researchers appreciate its ease of handling and the efficiency it brings to synthetic pathways, making it a preferred choice for those looking to streamline their processes. With its unique properties and broad applicability, this compound stands out as a crucial tool for professionals in both the pharmaceutical and materials industries.

Synonyms
2-Carbomethoxy-3-thiophenesulfonyl chloride, 3-(Chlorosulfonyl)-2-thiophenecarboxylic acid methyl ester, 2-(Methoxycarbonyl)-3-thiophenesulfonyl chloride
CAS Number
59337-92-7
Purity
≥ 90% (GC)
Molecular Formula
C6H5ClO4S2
Molecular Weight
240.67
MDL Number
MFCD00068160
PubChem ID
2736733
Melting Point
63 °C
Appearance
White to orange to green crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
2-Carbomethoxy-3-thiophenesulfonyl chloride, 3-(Chlorosulfonyl)-2-thiophenecarboxylic acid methyl ester, 2-(Methoxycarbonyl)-3-thiophenesulfonyl chloride
CAS Number
59337-92-7
Purity
≥ 90% (GC)
Molecular Formula
C6H5ClO4S2
Molecular Weight
240.67
MDL Number
MFCD00068160
PubChem ID
2736733
Melting Point
63 °C
Appearance
White to orange to green crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Methyl 3-(chlorosulfonyl)-2-thiophenecarboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly those targeting inflammatory diseases due to its unique sulfonyl group.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, including herbicides and fungicides, enhancing crop protection by targeting specific pests and pathogens.
  • Material Science: The compound is explored in the development of advanced materials, such as conductive polymers, which are essential in electronics and energy storage applications.
  • Organic Synthesis: Researchers utilize it as a building block in organic synthesis, allowing for the creation of complex molecules with diverse functional groups, which can lead to innovative products.
  • Analytical Chemistry: It is employed in analytical methods for detecting and quantifying thiophene derivatives, aiding in environmental monitoring and quality control in various industries.

Citations