4-(2-(piperidin-1-yl)ethoxy)aniline

95%

Reagent Code: #226959
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CAS Number 38948-27-5

science Other reagents with same CAS 38948-27-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.31 g/mol
Formula C₁₃H₂₀N₂O
badge Registry Numbers
MDL Number MFCD07365100
thermostat Physical Properties
Melting Point 67 °C
Boiling Point 377.1±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.070±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of selective estrogen receptor modulators (SERMs). It serves as a key building block in creating compounds with potential applications in hormone therapy and the treatment of hormone-related cancers. Its structure allows for functionalization that enhances binding affinity to estrogen receptors, making it valuable in medicinal chemistry research. Also employed in the preparation of dyes and functional materials due to its electron-donating aromatic amine group and flexible side chain.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,970.00
inventory 1g
10-20 days ฿7,590.00
inventory 5g
10-20 days ฿31,150.00
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4-(2-(piperidin-1-yl)ethoxy)aniline
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of selective estrogen receptor modulators (SERMs). It serves as a key building block in creating compounds with potential applications in hormone therapy and the treatment of hormone-related cancers. Its structure allows for functionalization that enhances binding affinity to estrogen receptors, making it valuable in medicinal chemistry research. Also employed in the preparation of dyes and functional materials due to

Used in the synthesis of pharmaceutical intermediates, particularly in the development of selective estrogen receptor modulators (SERMs). It serves as a key building block in creating compounds with potential applications in hormone therapy and the treatment of hormone-related cancers. Its structure allows for functionalization that enhances binding affinity to estrogen receptors, making it valuable in medicinal chemistry research. Also employed in the preparation of dyes and functional materials due to its electron-donating aromatic amine group and flexible side chain.

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