(6-Bromo-pyridin-3-ylmethyl)-cyclopropyl-aminehydrochloride

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Reagent Code: #152477
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CAS Number 1289387-50-3

science Other reagents with same CAS 1289387-50-3

blur_circular Chemical Specifications

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Weight 227.10 g/mol
Formula C₉H₁₁BrN₂
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MDL Number MFCD18837145
inventory_2 Storage & Handling
Density 1.50 g/cm3
Storage Room temperature, seal, dry

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 its ability to enhance binding selectivity and improve metabolic stability in drug candidates. Commonly employed in the preparation of pyridine-based analogs targeting neurological disorders and inflammatory diseases. Its bromo functionality allows for further cross-coupling reactions, enabling structural diversification in drug discovery programs.

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inventory 1g
10-20 days ฿34,120.00

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(6-Bromo-pyridin-3-ylmethyl)-cyclopropyl-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 its ability to enhance binding selectivity and improve metabolic stability in drug candidates. Commonly employed in the preparation of pyridine-based analogs targeting neurological disorders and inflammatory diseases. Its bromo functionality allows for further cross-coupling reactions, enabling struc

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 its ability to enhance binding selectivity and improve metabolic stability in drug candidates. Commonly employed in the preparation of pyridine-based analogs targeting neurological disorders and inflammatory diseases. Its bromo functionality allows for further cross-coupling reactions, enabling structural diversification in drug discovery programs.

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