2-Oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acid

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Reagent Code: #221524
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CAS Number 70639-77-9

science Other reagents with same CAS 70639-77-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.18 g/mol
Formula C₁₀H₉NO₃
thermostat Physical Properties
Melting Point 300°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antihypertensive agents and renin inhibitors. Its structure supports the creation of compounds that modulate enzyme activity involved in blood pressure regulation. Also employed in research for designing new bioactive molecules due to its fused ring system, which enhances binding affinity to biological targets. Shows potential in the preparation of nootropic and neuroprotective agents. Commonly utilized in medicinal chemistry for scaffold modification to improve pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿450.00
inventory 1g
10-20 days ฿1,200.00
inventory 5g
10-20 days ฿4,480.00

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2-Oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antihypertensive agents and renin inhibitors. Its structure supports the creation of compounds that modulate enzyme activity involved in blood pressure regulation. Also employed in research for designing new bioactive molecules due to its fused ring system, which enhances binding affinity to biological targets. Shows potential in the preparation of nootropic and neuroprotective agents. Commonly utilized in

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antihypertensive agents and renin inhibitors. Its structure supports the creation of compounds that modulate enzyme activity involved in blood pressure regulation. Also employed in research for designing new bioactive molecules due to its fused ring system, which enhances binding affinity to biological targets. Shows potential in the preparation of nootropic and neuroprotective agents. Commonly utilized in medicinal chemistry for scaffold modification to improve pharmacokinetic properties.

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