(4-Methoxy-3-phenylmethoxyphenyl)methanol

95%

Reagent Code: #210492
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CAS Number 1860-60-2

science Other reagents with same CAS 1860-60-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.29 g/mol
Formula C₁₅H₁₆O₃
badge Registry Numbers
MDL Number MFCD00183283
thermostat Physical Properties
Melting Point 70-71 °C
Boiling Point 395.6±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.152±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of central nervous system agents. It serves as a building block in the production of certain antidepressants and anxiolytic drugs due to its structural similarity to bioactive phenylalkylamine derivatives. Its hydroxyl and ether functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in research settings to study serotonin receptor ligands and their binding properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,010.00
inventory 250mg
10-20 days ฿5,840.00
inventory 1g
10-20 days ฿17,970.00
(4-Methoxy-3-phenylmethoxyphenyl)methanol
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of central nervous system agents. It serves as a building block in the production of certain antidepressants and anxiolytic drugs due to its structural similarity to bioactive phenylalkylamine derivatives. Its hydroxyl and ether functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in research settings to study serotonin recep

Used in the synthesis of pharmaceutical intermediates, particularly in the development of central nervous system agents. It serves as a building block in the production of certain antidepressants and anxiolytic drugs due to its structural similarity to bioactive phenylalkylamine derivatives. Its hydroxyl and ether functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in research settings to study serotonin receptor ligands and their binding properties.

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