Ethyl 4-(4-formyl-3-hydroxyphenoxy)butanoate

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Reagent Code: #183508
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CAS Number 152942-06-8

science Other reagents with same CAS 152942-06-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.26 g/mol
Formula C₁₃H₁₆O₅
badge Registry Numbers
MDL Number MFCD29765746
thermostat Physical Properties
Boiling Point 405.7±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of beta-blockers and other cardiovascular drugs. Its aldehyde and ester functional groups allow for further chemical modifications, making it valuable in constructing complex organic molecules. Commonly employed in research settings for creating analogs and derivatives in medicinal chemistry. Also utilized in the preparation of prodrugs due to the presence of hydrolyzable ester linkage, which can improve bioavailability.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿990.00
inventory 5g
10-20 days ฿3,850.00
inventory 25g
10-20 days ฿16,700.00
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Ethyl 4-(4-formyl-3-hydroxyphenoxy)butanoate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of beta-blockers and other cardiovascular drugs. Its aldehyde and ester functional groups allow for further chemical modifications, making it valuable in constructing complex organic molecules. Commonly employed in research settings for creating analogs and derivatives in medicinal chemistry. Also utilized in the preparation of prodrugs due to the presence of hydrolyzable ester linkage, which can improve bioavailabi
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of beta-blockers and other cardiovascular drugs. Its aldehyde and ester functional groups allow for further chemical modifications, making it valuable in constructing complex organic molecules. Commonly employed in research settings for creating analogs and derivatives in medicinal chemistry. Also utilized in the preparation of prodrugs due to the presence of hydrolyzable ester linkage, which can improve bioavailability.
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