(5-bromo-4-methylpyridin-2-yl)methanamine hydrochloride

≥95%

Reagent Code: #144000
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CAS Number 1257535-47-9

science Other reagents with same CAS 1257535-47-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.53 g/mol
Formula C₇H₉BrN₂·HCl
badge Registry Numbers
MDL Number MFCD17214201
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 targeted therapies. Commonly employed in medicinal chemistry for constructing more complex molecules due to its reactive amine group and halogenated aromatic ring, which enable further functionalization through cross-coupling reactions. Also utilized in research settings for the design of new bioactive molecules with potential neurological or anti-inflammatory activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,980.00
inventory 500mg
10-20 days ฿50,740.00

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(5-bromo-4-methylpyridin-2-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 targeted therapies. Commonly employed in medicinal chemistry for constructing more complex molecules due to its reactive amine group and halogenated aromatic ring, which enable further functionalization through cross-coupling reactions. Also utilized in research s

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 targeted therapies. Commonly employed in medicinal chemistry for constructing more complex molecules due to its reactive amine group and halogenated aromatic ring, which enable further functionalization through cross-coupling reactions. Also utilized in research settings for the design of new bioactive molecules with potential neurological or anti-inflammatory activity.

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