[1,2,4]Triazolo[1,5-a]pyrazin-2-amine

97%

Reagent Code: #241693
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CAS Number 88002-33-9

science Other reagents with same CAS 88002-33-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 135.13 g/mol
Formula C₅H₅N₅
badge Registry Numbers
MDL Number MFCD11847742
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in π-π stacking interactions, enhancing binding affinity to biological targets. Also employed in the design of CNS-active compounds owing to its favorable physicochemical properties and ability to cross the blood-brain barrier. Additionally, it finds use in agrochemicals for developing herbicides and fungicides, leveraging its heterocyclic structure for bioactivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿910.00
inventory 1g
10-20 days ฿2,680.00
inventory 5g
10-20 days ฿8,730.00
inventory 10g
10-20 days ฿16,560.00
[1,2,4]Triazolo[1,5-a]pyrazin-2-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in π-π stacking interactions, enhancing binding affinity to biological targets. Also employed in the design of CNS-active compounds owing to its favorable physicochemical properties and ability to cross the blood-brain barrier. Additionally, it finds use in agroch

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in π-π stacking interactions, enhancing binding affinity to biological targets. Also employed in the design of CNS-active compounds owing to its favorable physicochemical properties and ability to cross the blood-brain barrier. Additionally, it finds use in agrochemicals for developing herbicides and fungicides, leveraging its heterocyclic structure for bioactivity.

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