3-(Cyclopropylmethoxy)-4-hydroxybenzoic acid

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Reagent Code: #160776
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CAS Number 1243391-44-7

science Other reagents with same CAS 1243391-44-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.21 g/mol
Formula C₁₁H₁₂O₄
thermostat Physical Properties
Boiling Point 403.3±30.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of bioactive molecules by serving as a building block for modifying aromatic cores in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the cyclopropyl and hydroxy groups that influence metabolic stability and binding affinity. Also utilized in the preparation of ester and amide derivatives to enhance cell permeability in prodrug designs.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,980.00
inventory 250mg
10-20 days ฿17,550.00
inventory 1g
10-20 days ฿39,800.00

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3-(Cyclopropylmethoxy)-4-hydroxybenzoic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of bioactive molecules by serving as a building block for modifying aromatic cores in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the cyclopropyl and hydroxy groups that influence metabolic stability and binding affinity. Also utilized in the preparation of este

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of bioactive molecules by serving as a building block for modifying aromatic cores in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the cyclopropyl and hydroxy groups that influence metabolic stability and binding affinity. Also utilized in the preparation of ester and amide derivatives to enhance cell permeability in prodrug designs.

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