4-Methyl-1H-pyrrolo[2,3-b]pyridine

97%

Reagent Code: #207129
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CAS Number 824-24-8

science Other reagents with same CAS 824-24-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 132.16 g/mol
Formula C₈H₈N₂
badge Registry Numbers
MDL Number MFCD00956196
thermostat Physical Properties
Melting Point 125-126°C
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 in the development of anticancer agents. It serves as a building block for compounds targeting tyrosine kinases involved in tumor growth and signal transduction. Also employed in the design of selective inhibitors for neurological and inflammatory disorders due to its ability to cross the blood-brain barrier and modulate enzyme activity. Its structural similarity to purine bases makes it valuable in creating biologically active molecules with improved metabolic stability and binding affinity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿360.00
100mg
10-20 days ฿950.00
250mg
10-20 days ฿1,880.00
1g
10-20 days ฿7,360.00
5g
10-20 days ฿32,450.00
4-Methyl-1H-pyrrolo[2,3-b]pyridine
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of anticancer agents. It serves as a building block for compounds targeting tyrosine kinases involved in tumor growth and signal transduction. Also employed in the design of selective inhibitors for neurological and inflammatory disorders due to its ability to cross the blood-brain barrier and modulate enzyme activity. Its structural similarity to purine bases makes it valuable in

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of anticancer agents. It serves as a building block for compounds targeting tyrosine kinases involved in tumor growth and signal transduction. Also employed in the design of selective inhibitors for neurological and inflammatory disorders due to its ability to cross the blood-brain barrier and modulate enzyme activity. Its structural similarity to purine bases makes it valuable in creating biologically active molecules with improved metabolic stability and binding affinity.

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