(3,6-Dichloro-2-fluorophenyl)methanamine hydrochloride

95%

Reagent Code: #178485
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CAS Number 2109805-53-8

science Other reagents with same CAS 2109805-53-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.49 g/mol
Formula C₇H₇Cl₃FN
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of selective kinase inhibitors and other bioactive molecules. Its structure allows for functionalization in multi-step reactions, making it valuable in medicinal chemistry for constructing complex drug candidates. The amine group serves as a handle for coupling reactions, while the halogen atoms enable cross-coupling transformations such as Suzuki or Buchwald-Hartwig reactions. It is especially useful in the preparation of compounds targeting neurological disorders and inflammatory conditions. Due to its reactivity and stability as a hydrochloride salt, it is well-suited for storage and use in controlled synthetic environments.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿28,120.00
inventory 250mg
10-20 days ฿38,030.00

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(3,6-Dichloro-2-fluorophenyl)methanamine hydrochloride
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Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of selective kinase inhibitors and other bioactive molecules. Its structure allows for functionalization in multi-step reactions, making it valuable in medicinal chemistry for constructing complex drug candidates. The amine group serves as a handle for coupling reactions, while the halogen atoms enable cross-coupling transformations such as Suzuki or Buchwald-Hartwig reactions. It is especially usefu

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of selective kinase inhibitors and other bioactive molecules. Its structure allows for functionalization in multi-step reactions, making it valuable in medicinal chemistry for constructing complex drug candidates. The amine group serves as a handle for coupling reactions, while the halogen atoms enable cross-coupling transformations such as Suzuki or Buchwald-Hartwig reactions. It is especially useful in the preparation of compounds targeting neurological disorders and inflammatory conditions. Due to its reactivity and stability as a hydrochloride salt, it is well-suited for storage and use in controlled synthetic environments.

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