1H-Pyrrolo[3,2-c]pyridine-2-carboxylic acid

95%

Reagent Code: #196555
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Alias 5-Azaindole-2-carboxylic acid
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CAS Number 800401-65-4

science Other reagents with same CAS 800401-65-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 162.15 g/mol
Formula C₈H₆N₂O₂
badge Registry Numbers
MDL Number MFCD09743299
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting cancer-related enzymes. Its structure supports the development of compounds with high selectivity and potency in cell signaling pathways. Also explored in the design of anti-inflammatory and neuroprotective agents due to its ability to cross biological membranes and interact with central nervous system targets. Commonly utilized in medicinal chemistry for scaffold modification to enhance drug-like properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿580.00
inventory 250mg
10-20 days ฿1,040.00
inventory 1g
10-20 days ฿3,350.00
inventory 5g
10-20 days ฿15,680.00

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1H-Pyrrolo[3,2-c]pyridine-2-carboxylic acid
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting cancer-related enzymes. Its structure supports the development of compounds with high selectivity and potency in cell signaling pathways. Also explored in the design of anti-inflammatory and neuroprotective agents due to its ability to cross biological membranes and interact with central nervous system targets. Commonly utilized in medicinal chemistry for scaffold modification to enhanc

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting cancer-related enzymes. Its structure supports the development of compounds with high selectivity and potency in cell signaling pathways. Also explored in the design of anti-inflammatory and neuroprotective agents due to its ability to cross biological membranes and interact with central nervous system targets. Commonly utilized in medicinal chemistry for scaffold modification to enhance drug-like properties.

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