Methyl 5-(chlorosulfonyl)-1-methyl-1H-pyrrole-2-carboxylate

95%

  • Product Code: 71475
  CAS:    306936-53-8
Molecular Weight: 237.66 g./mol Molecular Formula: C₇H₈ClNO₄S
EC Number: MDL Number: MFCD02180789
Melting Point: 79 °C Boiling Point: 364.9°C at 760 mmHg
Density: 1.49±0.1 g/cm3 Storage Condition: 2-8°C
Product Description: This chemical is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its chlorosulfonyl group makes it a valuable reagent for introducing sulfonamide functionalities into target molecules, which are often found in drugs with antibacterial, antiviral, or anti-inflammatory properties. Additionally, its pyrrole ring structure contributes to its use in the development of heterocyclic compounds, which are significant in medicinal chemistry. The compound is also employed in research settings for the synthesis of complex organic molecules, particularly those requiring sulfonylation reactions. Its reactivity and structural features make it a versatile tool in the design and synthesis of biologically active compounds.
Product Specification:
Test Specification
APPEARANCE White to Yellow solid
PURITY 94.5-100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days Ft8,727.03
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0.250 10-20 days Ft21,332.73
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1.000 10-20 days Ft43,829.07
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Methyl 5-(chlorosulfonyl)-1-methyl-1H-pyrrole-2-carboxylate
This chemical is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its chlorosulfonyl group makes it a valuable reagent for introducing sulfonamide functionalities into target molecules, which are often found in drugs with antibacterial, antiviral, or anti-inflammatory properties. Additionally, its pyrrole ring structure contributes to its use in the development of heterocyclic compounds, which are significant in medicinal chemistry. The compound is also employed in research settings for the synthesis of complex organic molecules, particularly those requiring sulfonylation reactions. Its reactivity and structural features make it a versatile tool in the design and synthesis of biologically active compounds.
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