(5-bromo-2-fluoropyridin-3-yl)methanamine hydrochloride

≥95%

Reagent Code: #144117
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CAS Number 1432754-51-2

science Other reagents with same CAS 1432754-51-2

blur_circular Chemical Specifications

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Weight 241.49 g/mol
Formula C₆H₇BrClFN₂
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MDL Number MFCD24447575
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding in biological systems, making it valuable in creating active pharmaceutical ingredients (APIs) targeting specific signaling pathways. Commonly employed in medicinal chemistry for derivatization due to the presence of amine and halogen groups, which facilitate coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Also utilized in the preparation of radiolabeled analogs for use in drug discovery and metabolic studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿25,860.00
inventory 1g
10-20 days ฿88,960.00
inventory 100mg
10-20 days ฿14,470.00

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(5-bromo-2-fluoropyridin-3-yl)methanamine hydrochloride
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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. Its structure allows for selective binding in biological systems, making it valuable in creating active pharmaceutical ingredients (APIs) targeting specific signaling pathways. Commonly employed in medicinal chemistry for derivatization due to the presence of amine and halogen groups, which facilitate coupling reactions such as Suzuki or Buchwald-Hartwig amin

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding in biological systems, making it valuable in creating active pharmaceutical ingredients (APIs) targeting specific signaling pathways. Commonly employed in medicinal chemistry for derivatization due to the presence of amine and halogen groups, which facilitate coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Also utilized in the preparation of radiolabeled analogs for use in drug discovery and metabolic studies.

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