Ethyl 4-aminocinnamate

97.0%

Reagent Code: #181818
label
Alias 4-Aminocinnamic acid ethyl ester
fingerprint
CAS Number 5048-82-8

science Other reagents with same CAS 5048-82-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.23 g/mol
Formula C₁₁H₁₃NO₂
badge Registry Numbers
EC Number 225-747-1
MDL Number MFCD00017116
thermostat Physical Properties
Melting Point 70-74 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. Its structure allows for incorporation into more complex molecules, particularly those requiring cinnamate derivatives with functionalized side chains. It is also employed in the development of UV-absorbing compounds, making it useful in sunscreen formulations and photostabilizers. The amine group enables further derivatization, such as acylation or diazotization, which broadens its utility in creating dyes, fluorescent probes, and bioactive compounds. Additionally, it serves as a building block in the synthesis of certain anticancer and anti-inflammatory agents due to its ability to mimic natural phenolic acids.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿9,450.00
inventory 25g
10-20 days ฿26,620.00
inventory 100g
10-20 days ฿83,800.00
inventory 1g
10-20 days ฿2,520.00
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Ethyl 4-aminocinnamate
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. Its structure allows for incorporation into more complex molecules, particularly those requiring cinnamate derivatives with functionalized side chains. It is also employed in the development of UV-absorbing compounds, making it useful in sunscreen formulations and photostabilizers. The amine group enables further derivatization, such as acylation or diazotization, which broadens its utili

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. Its structure allows for incorporation into more complex molecules, particularly those requiring cinnamate derivatives with functionalized side chains. It is also employed in the development of UV-absorbing compounds, making it useful in sunscreen formulations and photostabilizers. The amine group enables further derivatization, such as acylation or diazotization, which broadens its utility in creating dyes, fluorescent probes, and bioactive compounds. Additionally, it serves as a building block in the synthesis of certain anticancer and anti-inflammatory agents due to its ability to mimic natural phenolic acids.

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