3-Methyl-2-thioxothiazolidin-4-one

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Reagent Code: #209805
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CAS Number 4807-55-0

science Other reagents with same CAS 4807-55-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.22 g/mol
Formula C₄H₅NOS₂
badge Registry Numbers
MDL Number MFCD00005490
thermostat Physical Properties
Melting Point 69-71 °C(lit.)
Boiling Point 213.4±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.344 (estimate)
Storage Room temperature, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and antimicrobial agents. It serves as a key building block in heterocyclic chemistry due to its reactive thiocarbonyl and active methylene groups, enabling the formation of various fused ring systems. Commonly employed in the preparation of thiazole and thiazolidine derivatives, which exhibit biological activity. Also applied in agrochemical research for developing novel plant growth regulators and pesticides. Its structural features make it valuable in medicinal chemistry for designing enzyme inhibitors.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿850.00
inventory 1g
10-20 days ฿2,120.00
inventory 5g
10-20 days ฿7,450.00

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3-Methyl-2-thioxothiazolidin-4-one
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and antimicrobial agents. It serves as a key building block in heterocyclic chemistry due to its reactive thiocarbonyl and active methylene groups, enabling the formation of various fused ring systems. Commonly employed in the preparation of thiazole and thiazolidine derivatives, which exhibit biological activity. Also applied in agrochemical research for developing novel plant growth regulators a

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and antimicrobial agents. It serves as a key building block in heterocyclic chemistry due to its reactive thiocarbonyl and active methylene groups, enabling the formation of various fused ring systems. Commonly employed in the preparation of thiazole and thiazolidine derivatives, which exhibit biological activity. Also applied in agrochemical research for developing novel plant growth regulators and pesticides. Its structural features make it valuable in medicinal chemistry for designing enzyme inhibitors.

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