(3-bromo-6-chloropyridin-2-yl)methanol

≥95%

Reagent Code: #144025
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CAS Number 1227601-71-9

science Other reagents with same CAS 1227601-71-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.47 g/mol
Formula C₆H₅BrClNO
badge Registry Numbers
MDL Number MFCD11847140
thermostat Physical Properties
Boiling Point 291.6±35.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It serves as a building block in agrochemicals for creating novel pesticides due to the presence of halogen atoms that facilitate further functionalization. The hydroxyl group allows for coupling reactions or conversion into esters and ethers, enabling its use in multi-step organic syntheses. Its structure supports selective transformations useful in medicinal chemistry for optimizing drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿3,690.00
5g
10-20 days ฿17,470.00
10g
10-20 days ฿32,140.00
25g
10-20 days ฿57,740.00
250mg
10-20 days ฿1,040.00
(3-bromo-6-chloropyridin-2-yl)methanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It serves as a building block in agrochemicals for creating novel pesticides due to the presence of halogen atoms that facilitate further functionalization. The hydroxyl group allows for coupling reactions or conversion into esters and ethers, enabling its use in multi-step organic syntheses. Its structure supports selective transformations useful in medicinal ch

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It serves as a building block in agrochemicals for creating novel pesticides due to the presence of halogen atoms that facilitate further functionalization. The hydroxyl group allows for coupling reactions or conversion into esters and ethers, enabling its use in multi-step organic syntheses. Its structure supports selective transformations useful in medicinal chemistry for optimizing drug candidates.

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