Lawesson reagent

97%

  • Product Code: 126635
  Alias:    Lowe's reagent, Lewis reagent, 2,4-bis(4-methoxyphenyl)-1,3-dithio-2,4-diphospho-2,4-sulfide
  CAS:    19172-47-5
Molecular Weight: 404.47 g./mol Molecular Formula: C₁₄H₁₄O₂P₂S₄
EC Number: 242-855-4 MDL Number: MFCD00005171
Melting Point: 228-230 °C(lit.) Boiling Point:
Density: Storage Condition: Room temperature, dry, inert gas atmosphere
Product Description: Lawesson reagent is widely used in organic synthesis for the thionation of carbonyl compounds, converting them into their corresponding thio-carbonyl derivatives. It is particularly valuable in the preparation of thioamides, thioketones, and thioesters, which are important intermediates in pharmaceutical and agrochemical industries. The reagent is also employed in the synthesis of heterocyclic compounds, such as thiophenes, which are key structures in many bioactive molecules. Additionally, it finds application in the modification of peptides and proteins by introducing sulfur-containing functional groups, enhancing their biological activity or stability. Its versatility and efficiency make it a crucial tool in the development of sulfur-containing organic compounds.
Product Specification:
Test Specification
Carbon 40.1-43
Melting Point 220-226
Purity (Ca) 97-102.5
Appearance Light Yellow To Brown Powder
Infrared Spectrum Conforms To Structure
Proton Nmr Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿290.00
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25.000 10-20 days ฿660.00
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100.000 10-20 days ฿1,410.00
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500.000 10-20 days ฿5,340.00
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2500.000 10-20 days ฿25,820.00
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Lawesson reagent
Lawesson reagent is widely used in organic synthesis for the thionation of carbonyl compounds, converting them into their corresponding thio-carbonyl derivatives. It is particularly valuable in the preparation of thioamides, thioketones, and thioesters, which are important intermediates in pharmaceutical and agrochemical industries. The reagent is also employed in the synthesis of heterocyclic compounds, such as thiophenes, which are key structures in many bioactive molecules. Additionally, it finds application in the modification of peptides and proteins by introducing sulfur-containing functional groups, enhancing their biological activity or stability. Its versatility and efficiency make it a crucial tool in the development of sulfur-containing organic compounds.
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