(6-Bromo-5-methoxypyridin-2-yl)methanol

95%

Reagent Code: #140980
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CAS Number 905562-91-6

science Other reagents with same CAS 905562-91-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.05 g/mol
Formula C₇H₈BrNO₂
badge Registry Numbers
MDL Number MFCD09702159
thermostat Physical Properties
Boiling Point 325.8±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.595±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its functional groups—bromine, methoxy, and hydroxymethyl—allow for selective modifications, enabling coupling reactions, ether formations, and nucleophilic substitutions. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems targeting neurological disorders and inflammatory diseases. Also utilized in agrochemical research for designing novel active ingredients due to its structural versatility.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,530.00
inventory 1g
10-20 days ฿20,790.00

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(6-Bromo-5-methoxypyridin-2-yl)methanol
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its functional groups—bromine, methoxy, and hydroxymethyl—allow for selective modifications, enabling coupling reactions, ether formations, and nucleophilic substitutions. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems targeting neurological disorders and inflammatory diseases. Also utilized in agroch

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its functional groups—bromine, methoxy, and hydroxymethyl—allow for selective modifications, enabling coupling reactions, ether formations, and nucleophilic substitutions. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems targeting neurological disorders and inflammatory diseases. Also utilized in agrochemical research for designing novel active ingredients due to its structural versatility.

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