1-(6-Chloro-4-methylpyridin-3-yl)ethan-1-ol

95%

Reagent Code: #163640
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CAS Number 1355200-45-1

science Other reagents with same CAS 1355200-45-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.62 g/mol
Formula C₈H₁₀ClNO
thermostat Physical Properties
Boiling Point 305.3±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.208±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. It serves as a building block in medicinal chemistry due to its functionalized pyridine core, which enhances binding selectivity in biological systems. Also employed in agrochemical research for designing novel pesticides with improved environmental profiles. Its hydroxyl and chloro-methyl substitution pattern allows for further chemical modifications, making it valuable in structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,660.00
inventory 250mg
10-20 days ฿43,330.00

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1-(6-Chloro-4-methylpyridin-3-yl)ethan-1-ol
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. It serves as a building block in medicinal chemistry due to its functionalized pyridine core, which enhances binding selectivity in biological systems. Also employed in agrochemical research for designing novel pesticides with improved environmental profiles. Its hydroxyl and chloro-methyl substitution pattern allows for further chemical modifications,

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. It serves as a building block in medicinal chemistry due to its functionalized pyridine core, which enhances binding selectivity in biological systems. Also employed in agrochemical research for designing novel pesticides with improved environmental profiles. Its hydroxyl and chloro-methyl substitution pattern allows for further chemical modifications, making it valuable in structure-activity relationship (SAR) studies.

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