2-(Methylthio)indolizine

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Reagent Code: #202971
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CAS Number 123471-47-6

science Other reagents with same CAS 123471-47-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.24 g/mol
Formula C₉H₉NS
badge Registry Numbers
MDL Number MFCD28678840
thermostat Physical Properties
Melting Point 67 °C
inventory_2 Storage & Handling
Density 1.12±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of compounds with potential anticancer and antimicrobial properties. Its structural framework supports the design of kinase inhibitors and receptor antagonists. Also explored in agrochemicals for creating novel pesticides due to its stability and reactivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies involving indolizine derivatives.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,120.00
inventory 250mg
10-20 days ฿30,150.00
inventory 1g
10-20 days ฿65,280.00

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2-(Methylthio)indolizine
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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of compounds with potential anticancer and antimicrobial properties. Its structural framework supports the design of kinase inhibitors and receptor antagonists. Also explored in agrochemicals for creating novel pesticides due to its stability and reactivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies involving indolizine derivatives

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of compounds with potential anticancer and antimicrobial properties. Its structural framework supports the design of kinase inhibitors and receptor antagonists. Also explored in agrochemicals for creating novel pesticides due to its stability and reactivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies involving indolizine derivatives.

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