Tert-butyl 6-chloropyridazin-3-ylcarbamate

95%

Reagent Code: #240181
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CAS Number 1276056-86-0

science Other reagents with same CAS 1276056-86-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.67 g/mol
Formula C₉H₁₂ClN₃O₂
badge Registry Numbers
MDL Number MFCD18070957
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to the reactivity of the chloropyridazine ring, enabling coupling reactions to form more complex molecules. Its tert-butyl carbamate group acts as a protecting group for amines, allowing selective functionalization during multi-step syntheses. Commonly employed in research settings for designing bioactive molecules with potential antitumor and anti-inflammatory activities.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,330.00
inventory 1g
10-20 days ฿3,120.00
inventory 5g
10-20 days ฿13,270.00
inventory 25g
10-20 days ฿45,410.00

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Tert-butyl 6-chloropyridazin-3-ylcarbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to the reactivity of the chloropyridazine ring, enabling coupling reactions to form more complex molecules. Its tert-butyl carbamate group acts as a protecting group for amines, allowing selective functionalization during multi-step syntheses. Commonly employed in research settings for designing bioactive

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to the reactivity of the chloropyridazine ring, enabling coupling reactions to form more complex molecules. Its tert-butyl carbamate group acts as a protecting group for amines, allowing selective functionalization during multi-step syntheses. Commonly employed in research settings for designing bioactive molecules with potential antitumor and anti-inflammatory activities.

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