2,2-Dimethyl-1-(2-Thioxothiazolidin-3-Yl)Propan-1-One

95%

Reagent Code: #177422
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CAS Number 138459-91-3

science Other reagents with same CAS 138459-91-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.32 g/mol
Formula C₈H₁₃NOS₂
badge Registry Numbers
MDL Number MFCD17392907
thermostat Physical Properties
Boiling Point 279.7±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.22±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals with potential antimicrobial and anti-inflammatory properties. It plays a role in constructing heterocyclic systems important in medicinal chemistry. Its thioxothiazolidine moiety contributes to reactivity useful in forming sulfur- and nitrogen-containing rings found in some drug candidates. Also explored in agrochemical research for designing novel pesticides and herbicides due to its ability to modulate enzyme activity in target organisms.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿8,900.00
250mg
10-20 days ฿16,070.00
1g
10-20 days ฿29,550.00
2,2-Dimethyl-1-(2-Thioxothiazolidin-3-Yl)Propan-1-One
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals with potential antimicrobial and anti-inflammatory properties. It plays a role in constructing heterocyclic systems important in medicinal chemistry. Its thioxothiazolidine moiety contributes to reactivity useful in forming sulfur- and nitrogen-containing rings found in some drug candidates. Also explored in agrochemical research for designing novel pesticides and herbicides due t

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals with potential antimicrobial and anti-inflammatory properties. It plays a role in constructing heterocyclic systems important in medicinal chemistry. Its thioxothiazolidine moiety contributes to reactivity useful in forming sulfur- and nitrogen-containing rings found in some drug candidates. Also explored in agrochemical research for designing novel pesticides and herbicides due to its ability to modulate enzyme activity in target organisms.

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