2-(Chloromethyl)-3,5-dimethylpyridin-4-ol

95%

Reagent Code: #162898
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CAS Number 220771-03-9

science Other reagents with same CAS 220771-03-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.62 g/mol
Formula C₈H₁₀ClNO
badge Registry Numbers
MDL Number MFCD13192038
inventory_2 Storage & Handling
Storage -20℃, avoid light, and store inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators. Its structure allows for functionalization at multiple sites, making it valuable in creating biologically active compounds. Commonly employed in the preparation of pyridine-based drugs where the chloromethyl group enables alkylation or coupling reactions. Also utilized in agrochemical research for designing novel pesticides with targeted activity. The hydroxyl and chloromethyl groups provide reactivity for esterification, ether formation, or nucleophilic substitution, supporting its role in building complex molecules.

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Test Parameter Specification
Appearance White to Off-White Solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,550.00
inventory 1g
10-20 days ฿24,550.00
inventory 250mg
10-20 days ฿9,880.00

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2-(Chloromethyl)-3,5-dimethylpyridin-4-ol
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators. Its structure allows for functionalization at multiple sites, making it valuable in creating biologically active compounds. Commonly employed in the preparation of pyridine-based drugs where the chloromethyl group enables alkylation or coupling reactions. Also utilized in agrochemical research for designing novel pesticides with targeted activity. The hydroxyl and chloromethyl gr

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators. Its structure allows for functionalization at multiple sites, making it valuable in creating biologically active compounds. Commonly employed in the preparation of pyridine-based drugs where the chloromethyl group enables alkylation or coupling reactions. Also utilized in agrochemical research for designing novel pesticides with targeted activity. The hydroxyl and chloromethyl groups provide reactivity for esterification, ether formation, or nucleophilic substitution, supporting its role in building complex molecules.

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