tert-Butyl 2-amino-6,7-dihydrothiazolo[5,4-c]pyridine-5(4H)-carboxylate

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Reagent Code: #145705
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CAS Number 365996-05-0

science Other reagents with same CAS 365996-05-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.34 g/mol
Formula C₁₁H₁₇N₃O₂S
thermostat Physical Properties
Boiling Point 412.8°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports the formation of biologically active molecules targeting inflammatory diseases and certain cancers. Commonly employed in medicinal chemistry for constructing heterocyclic scaffolds with enhanced binding affinity to protein targets. Also utilized in research settings to explore new therapeutic agents due to its favorable reactivity and stability in multi-step organic transformations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿181.50
inventory 1g
10-20 days ฿577.50
inventory 5g
10-20 days ฿4,250.00
inventory 10g
10-20 days ฿8,500.00
inventory 25g
10-20 days ฿17,710.00

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tert-Butyl 2-amino-6,7-dihydrothiazolo[5,4-c]pyridine-5(4H)-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports the formation of biologically active molecules targeting inflammatory diseases and certain cancers. Commonly employed in medicinal chemistry for constructing heterocyclic scaffolds with enhanced binding affinity to protein targets. Also utilized in research settings to explore new therapeutic agents due to its favorable reactivity and stability in multi-ste

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports the formation of biologically active molecules targeting inflammatory diseases and certain cancers. Commonly employed in medicinal chemistry for constructing heterocyclic scaffolds with enhanced binding affinity to protein targets. Also utilized in research settings to explore new therapeutic agents due to its favorable reactivity and stability in multi-step organic transformations.

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