Methyl 2-amino-4-(benzyloxy)-5-methoxybenzoate

95%

Reagent Code: #208668
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CAS Number 61032-42-6

science Other reagents with same CAS 61032-42-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.31 g/mol
Formula C₁₆H₁₇NO₄
badge Registry Numbers
MDL Number MFCD16620533
thermostat Physical Properties
Boiling Point 450°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed from light

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to prepare analogs for structure-activity relationship (SAR) studies. Also utilized in the preparation of fluorescent probes and labeled compounds due to the presence of modifiable amino and ether groups.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿800.00
inventory 1g
10-20 days ฿2,340.00
inventory 5g
10-20 days ฿10,720.00
inventory 10g
10-20 days ฿18,610.00

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Methyl 2-amino-4-(benzyloxy)-5-methoxybenzoate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to prepare analogs for structure-activity relationship (SAR) studies. Also utilized in the preparation of fluorescent probes and labeled compounds due to the presence of modifiable a

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to prepare analogs for structure-activity relationship (SAR) studies. Also utilized in the preparation of fluorescent probes and labeled compounds due to the presence of modifiable amino and ether groups.

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