(6-Chloro-4-methylpyridin-3-yl)methanol

98%

Reagent Code: #163439
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CAS Number 1263060-05-4

science Other reagents with same CAS 1263060-05-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.6 g/mol
Formula C₇H₈ClNO
badge Registry Numbers
MDL Number MFCD21090245
thermostat Physical Properties
Boiling Point 304.3±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.263±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals for creating herbicides and insecticides due to its pyridine core, which enhances bioavailability and binding affinity. Also employed in research for modifying bioactive molecules, leveraging the hydroxyl and chloro groups for further functionalization. Its structure supports cross-coupling reactions, making it valuable in medicinal chemistry for generating compound libraries.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,070.00
inventory 250mg
10-20 days ฿4,960.00
inventory 1g
10-20 days ฿18,810.00

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(6-Chloro-4-methylpyridin-3-yl)methanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals for creating herbicides and insecticides due to its pyridine core, which enhances bioavailability and binding affinity. Also employed in research for modifying bioactive molecules, leveraging the hydroxyl and chloro groups for further functionalization. Its structure supports cross-coupling reactions, making it valuable i

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals for creating herbicides and insecticides due to its pyridine core, which enhances bioavailability and binding affinity. Also employed in research for modifying bioactive molecules, leveraging the hydroxyl and chloro groups for further functionalization. Its structure supports cross-coupling reactions, making it valuable in medicinal chemistry for generating compound libraries.

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