4916-55-6

Usage

Uses

Used in Chemical Synthesis:
3-(Bromomethyl)pyridine is used as a synthetic building block for the creation of various organic compounds. Its bromine atom allows for further functionalization and reactions, making it a versatile starting material in the synthesis of complex molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(Bromomethyl)pyridine is used as a key intermediate in the development of new drugs. Its unique structure and reactivity enable the formation of novel compounds with potential therapeutic applications.
Used in Material Science:
3-(Bromomethyl)pyridine is also utilized in material science for the synthesis of specialty polymers and other advanced materials. Its ability to form covalent bonds with a variety of substrates makes it a valuable component in the development of new materials with specific properties.
Used in the Preparation of Ether Ligands:
3-(Bromomethyl)pyridine hydrobromide may be used in the preparation of ether ligands, which are important in various chemical applications, including catalysis and the formation of coordination complexes. The bromodimethyl group in 3-(Bromomethyl)pyridine allows for the easy formation of ether linkages, making it a suitable candidate for this purpose.

InChI:InChI=1/C6H6BrN.BrH/c7-4-6-2-1-3-8-5-6;/h1-3,5H,4H2;1H

Upstream product

• 93-60-7 methyl 3-pyridinecarboxylate 
• 100-55-0 3-hydroxymethylpyridin 

Downstream Products

• 108-99-6 3-Methylpyridine 
• 1586781-78-3 N'-[(tert-butoxy)carbonyl]-N-(pyridin-3-ylmethyl)(tert-butoxy)carbohydrazide 
• 1436855-80-9 methyl 2-tert-butoxy-2-(4-(4-chlorophenyl)-2,3,6-trimethyl-1-(pyridin-3-ylmethyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)acetate 
• 1099598-09-0 3-(2,2,2-trifluoroethyl)pyridine 
• 864754-21-2 3-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methyl)pyridine 
• 1253731-85-9 2-(4-hydroxy-3,5-dimethylphenyl)-5-methoxy-7-[2-(pyridin-3-ylmethoxy)ethoxy]-3H-quinazolin-4-one 

Relevant academic research and scientific papers

Novel supramolecular charge-transfer systems based on bis(18-crown-6) stilbene and viologen analogues bearing two ammonioalkylgroups

A series of new viologen analogues bearing two ammonioalkyl groups (2-4) were synthesized in order to study their complexation with bis(18-crown-6) stilbene (1b). Electronic spectroscopy and 1H NMR measurements show that in acetonitrile, bis(cr

PIPERIDINONES USEFUL IN THE TREATMENT OF INFLAMMATION

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13C NMR SPECTRAL AND STEREOCHEMICAL ANALYSIS OF PIPERIDINE DERIVED α-AMINONITRILES

Carbon-13 NMR spectra of several α-aminonitriles are reported, along with their preparation via the modified Polonovski reaction or the reductive cyanation of Fry.The substituent effects for the cyano group in the different nitrogen heterocycles were dete