Lawesson reagent
97%
Reagent
Code: #126635
Alias
Lowe's reagent, Lewis reagent, 2,4-bis(4-methoxyphenyl)-1,3-dithio-2,4-diphospho-2,4-sulfide
CAS Number
19172-47-5
blur_circular Chemical Specifications
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Molecular Information
Weight
404.47 g/mol
Formula
C₁₄H₁₄O₂P₂S₄
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Registry Numbers
EC Number
242-855-4
MDL Number
MFCD00005171
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Physical Properties
Melting Point
228-230 °C(lit.)
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Storage & Handling
Storage
Room temperature, dry, inert gas atmosphere
description 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.
format_list_bulleted Product Specification
Test Parameter | 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 |
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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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