4-BENZYLOXY-3-CHLOROANILINE

95%

Reagent Code: #149555
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CAS Number 59404-86-3

science Other reagents with same CAS 59404-86-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.69 g/mol
Formula C₁₃H₁₂ClNO
badge Registry Numbers
MDL Number MFCD03427265
thermostat Physical Properties
Melting Point 56-60 °C (lit.)
Boiling Point 390.6±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.240±0.06 g/cm3(Predicted)
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. It serves as a building block in the development of bioactive molecules due to the presence of both amine and ether functionalities, which allow for further chemical modifications. Its chloro and benzyloxy groups provide sites for cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex drug scaffolds. Also employed in the preparation of agrochemicals and functional dyes where aromatic amines are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿920.00

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4-BENZYLOXY-3-CHLOROANILINE
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. It serves as a building block in the development of bioactive molecules due to the presence of both amine and ether functionalities, which allow for further chemical modifications. Its chloro and benzyloxy groups provide sites for cross-coupling reactions, making it valuable in medicinal chemistry for constructing comple

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. It serves as a building block in the development of bioactive molecules due to the presence of both amine and ether functionalities, which allow for further chemical modifications. Its chloro and benzyloxy groups provide sites for cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex drug scaffolds. Also employed in the preparation of agrochemicals and functional dyes where aromatic amines are required.

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