1-(6-Bromopyridin-2-yl)ethan-1-aminehydrochloride

98%

Reagent Code: #155049
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CAS Number 1415257-60-1

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.52 g/mol
Formula C₇H₁₀BrClN₂
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 for cancer treatment. It serves as a building block in medicinal chemistry due to the presence of both bromine and amine functional groups, which allow for further chemical modifications through cross-coupling reactions and amide bond formations. Commonly employed in the preparation of biologically active molecules targeting neurological disorders and inflammatory diseases. Its hydrochloride salt form enhances solubility and stability, making it suitable for use in aqueous reaction conditions and purification processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,860.00
inventory 250mg
10-20 days ฿11,180.00
inventory 1g
10-20 days ฿22,670.00
inventory 5g
10-20 days ฿34,690.00
inventory 10g
10-20 days ฿64,960.00

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1-(6-Bromopyridin-2-yl)ethan-1-aminehydrochloride
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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. It serves as a building block in medicinal chemistry due to the presence of both bromine and amine functional groups, which allow for further chemical modifications through cross-coupling reactions and amide bond formations. Commonly employed in the preparation of biologically active molecules targeting neurological disorders and inflammatory diseases. Its hy

Used as a key 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 presence of both bromine and amine functional groups, which allow for further chemical modifications through cross-coupling reactions and amide bond formations. Commonly employed in the preparation of biologically active molecules targeting neurological disorders and inflammatory diseases. Its hydrochloride salt form enhances solubility and stability, making it suitable for use in aqueous reaction conditions and purification processes.

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