2-(1H-Pyrrolo[3,2-c]pyridin-3-yl)ethanamine

≥95%

Reagent Code: #195587
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CAS Number 1778-74-1

science Other reagents with same CAS 1778-74-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.20 g/mol
Formula C₉H₁₁N₃
badge Registry Numbers
MDL Number MFCD16657175
thermostat Physical Properties
Boiling Point 376°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.225g/cm3
Storage 2-8°C, dry and sealed from light

description Product Description

Used in pharmaceutical research as a key intermediate for synthesizing kinase inhibitors, particularly in the development of targeted cancer therapies. It shows potential in modulating signaling pathways involved in cell proliferation and survival. Due to its structural similarity to purine bases, it can interact with ATP-binding sites in enzymes, making it valuable in designing drugs for oncology and inflammatory diseases. Also explored in the synthesis of neuroactive compounds due to its ability to cross the blood-brain barrier and influence neurotransmitter systems.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿28,260.00
2-(1H-Pyrrolo[3,2-c]pyridin-3-yl)ethanamine
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Used in pharmaceutical research as a key intermediate for synthesizing kinase inhibitors, particularly in the development of targeted cancer therapies. It shows potential in modulating signaling pathways involved in cell proliferation and survival. Due to its structural similarity to purine bases, it can interact with ATP-binding sites in enzymes, making it valuable in designing drugs for oncology and inflammatory diseases. Also explored in the synthesis of neuroactive compounds due to its ability to cro

Used in pharmaceutical research as a key intermediate for synthesizing kinase inhibitors, particularly in the development of targeted cancer therapies. It shows potential in modulating signaling pathways involved in cell proliferation and survival. Due to its structural similarity to purine bases, it can interact with ATP-binding sites in enzymes, making it valuable in designing drugs for oncology and inflammatory diseases. Also explored in the synthesis of neuroactive compounds due to its ability to cross the blood-brain barrier and influence neurotransmitter systems.

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