(6-Chloro-5-iodopyridin-3-yl)methanol

98%

Reagent Code: #74235
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CAS Number 1360938-13-1

science Other reagents with same CAS 1360938-13-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.47 g/mol
Formula C₆H₅ClINO
thermostat Physical Properties
Boiling Point 367.6±42.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the preparation of more complex molecules. Its structure, featuring both chloro and iodo substituents on the pyridine ring, makes it a versatile building block for constructing heterocyclic compounds. It is often employed in pharmaceutical research for the development of potential drug candidates, particularly in the synthesis of molecules with biological activity. Additionally, its reactive sites allow for further functionalization, enabling the creation of diverse chemical entities for use in material science and agrochemical industries. The presence of the hydroxyl group also facilitates its use in coupling reactions, making it valuable in the production of specialized polymers and ligands for catalysis.

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Test Parameter Specification
Appearance Report Result
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿459.00
inventory 250mg
10-20 days ฿1,188.00
inventory 1g
10-20 days ฿3,195.00
inventory 5g
10-20 days ฿9,531.00

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(6-Chloro-5-iodopyridin-3-yl)methanol
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This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the preparation of more complex molecules. Its structure, featuring both chloro and iodo substituents on the pyridine ring, makes it a versatile building block for constructing heterocyclic compounds. It is often employed in pharmaceutical research for the development of potential drug candidates, particularly in the synthesis of molecules with biological activity. Additionally, its reactive si

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the preparation of more complex molecules. Its structure, featuring both chloro and iodo substituents on the pyridine ring, makes it a versatile building block for constructing heterocyclic compounds. It is often employed in pharmaceutical research for the development of potential drug candidates, particularly in the synthesis of molecules with biological activity. Additionally, its reactive sites allow for further functionalization, enabling the creation of diverse chemical entities for use in material science and agrochemical industries. The presence of the hydroxyl group also facilitates its use in coupling reactions, making it valuable in the production of specialized polymers and ligands for catalysis.

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