3',4',5'-Trimethoxyacetophenone

98%

Reagent Code: #240638
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CAS Number 1136-86-3

science Other reagents with same CAS 1136-86-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.23 g/mol
Formula C₁₁H₁₄O₄
badge Registry Numbers
MDL Number MFCD00008738
thermostat Physical Properties
Melting Point 78-80°C (Lit.)
Boiling Point 173-174°C/10mm Hg (Lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of vasodilator drugs and certain antiarrhythmic agents. It plays a key role in constructing complex organic molecules due to the reactivity of the ketone group and the electron-donating methoxy substituents. Commonly employed in research settings for developing bioactive compounds and in the preparation of natural product analogs. Its structural features make it valuable in medicinal chemistry for optimizing drug candidates with improved metabolic stability and binding affinity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿350.00
inventory 5g
10-20 days ฿940.00
inventory 25g
10-20 days ฿4,330.00
inventory 100g
10-20 days ฿16,480.00

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3',4',5'-Trimethoxyacetophenone
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of vasodilator drugs and certain antiarrhythmic agents. It plays a key role in constructing complex organic molecules due to the reactivity of the ketone group and the electron-donating methoxy substituents. Commonly employed in research settings for developing bioactive compounds and in the preparation of natural product analogs. Its structural features make it valuable in medicinal chemistry for optimizing drug

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of vasodilator drugs and certain antiarrhythmic agents. It plays a key role in constructing complex organic molecules due to the reactivity of the ketone group and the electron-donating methoxy substituents. Commonly employed in research settings for developing bioactive compounds and in the preparation of natural product analogs. Its structural features make it valuable in medicinal chemistry for optimizing drug candidates with improved metabolic stability and binding affinity.

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