Lawesson reagent

97%

Reagent Code: #126635
label
Alias Lowe's reagent, Lewis reagent, 2,4-bis(4-methoxyphenyl)-1,3-dithio-2,4-diphospho-2,4-sulfide
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CAS Number 19172-47-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 404.47 g/mol
Formula C₁₄H₁₄O₂P₂S₄
badge Registry Numbers
EC Number 242-855-4
MDL Number MFCD00005171
thermostat Physical Properties
Melting Point 228-230 °C(lit.)
inventory_2 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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿1,410.00
inventory 2.5kg
10-20 days ฿25,820.00
inventory 5g
10-20 days ฿290.00
inventory 25g
10-20 days ฿660.00
inventory 500g
10-20 days ฿5,340.00
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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