2-(Bromomethyl)-3-(trifluoromethyl)pyridine hydrobromide

≥95%

Reagent Code: #79110
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CAS Number 1956318-54-9

science Other reagents with same CAS 1956318-54-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.93 g/mol
Formula C₇H₆Br₂F₃N
badge Registry Numbers
MDL Number MFCD27923458
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. Its reactive bromomethyl group allows for facile functionalization, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. The trifluoromethyl group enhances the compound's lipophilicity, which is beneficial in drug design for improving bioavailability and metabolic stability. It is often employed in cross-coupling reactions, nucleophilic substitutions, and as an intermediate in the preparation of pyridine derivatives with potential biological activity. Additionally, its use in material science is explored for creating advanced polymers and coatings with specific properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,250.00
inventory 250mg
10-20 days ฿22,500.00

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2-(Bromomethyl)-3-(trifluoromethyl)pyridine hydrobromide
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This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. Its reactive bromomethyl group allows for facile functionalization, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. The trifluoromethyl group enhances the compound's lipophilicity, which is beneficial in drug design for improving bioavailability and metabolic stability. It is often employed in cross-coupling reactio

This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. Its reactive bromomethyl group allows for facile functionalization, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. The trifluoromethyl group enhances the compound's lipophilicity, which is beneficial in drug design for improving bioavailability and metabolic stability. It is often employed in cross-coupling reactions, nucleophilic substitutions, and as an intermediate in the preparation of pyridine derivatives with potential biological activity. Additionally, its use in material science is explored for creating advanced polymers and coatings with specific properties.

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