3-(6-Bromopyridin-3-yl)propan-1-ol

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Reagent Code: #74416
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CAS Number 656827-76-8

science Other reagents with same CAS 656827-76-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.08 g/mol
Formula C₈H₁₀BrNO
badge Registry Numbers
MDL Number MFCD20040447
thermostat Physical Properties
Boiling Point 336.6±27.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological disorders. Additionally, it is employed in the synthesis of ligands for catalytic processes, enhancing efficiency in chemical reactions. Its bromine substituent allows for further functionalization, making it versatile in creating specialized compounds for research and industrial applications.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,570.00
inventory 250mg
10-20 days ฿7,720.00

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3-(6-Bromopyridin-3-yl)propan-1-ol
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological disorders. Additionally, it is employed in the synthesis of ligands for catalytic processes, enhancing efficiency in chemical reactions. Its bromine substituent allows for further functionalization, making it versatile in creating sp

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological disorders. Additionally, it is employed in the synthesis of ligands for catalytic processes, enhancing efficiency in chemical reactions. Its bromine substituent allows for further functionalization, making it versatile in creating specialized compounds for research and industrial applications.

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