6-(4-Methylpiperazin-1-yl)pyridazin-3-amine

≥95%

Reagent Code: #208951
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CAS Number 66346-94-9

science Other reagents with same CAS 66346-94-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.25 g/mol
Formula C₉H₁₅N₅
badge Registry Numbers
MDL Number MFCD13192341
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables effective binding to enzyme active sites, making it valuable in drug design for targeted therapies. Also explored in the creation of anti-inflammatory and antimicrobial agents due to its favorable interaction with biological targets. Commonly utilized in research settings for structure-activity relationship (SAR) studies to optimize drug potency and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,920.00
inventory 1g
10-20 days ฿17,160.00
inventory 5g
10-20 days ฿38,780.00
inventory 250mg
10-20 days ฿6,850.00

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6-(4-Methylpiperazin-1-yl)pyridazin-3-amine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables effective binding to enzyme active sites, making it valuable in drug design for targeted therapies. Also explored in the creation of anti-inflammatory and antimicrobial agents due to its favorable interaction with biological targets. Commonly utilized in research settings for structure-activity relationship (SAR) studies to optimize drug

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables effective binding to enzyme active sites, making it valuable in drug design for targeted therapies. Also explored in the creation of anti-inflammatory and antimicrobial agents due to its favorable interaction with biological targets. Commonly utilized in research settings for structure-activity relationship (SAR) studies to optimize drug potency and selectivity.

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