Chemistry Organic Building Blocks Fluorinated Building Blocks 2,6-difluorobenzoic acid
These compounds have the same murcko framework: benzene,and at least 2 kinds of functional groups( —F,—COOH).
Metalation Reactions: Fluorobenzene can undergo metalation reactions, where a metal species (such as an organolithium or organomagnesium compound) replaces a hydrogen atom on the benzene ring. These metalated intermediates can then be used in various synthetic transformations.
Neutralization Reaction with Bases: Benzoic acid can react with bases to form water-soluble salts called benzoates. The reaction is a typical acid-base neutralization reaction, where the hydrogen ion from the carboxylic acid group is replaced by a metal cation or another positively charged organic group.
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8-Bromo-6-fluoro-[1,2,4]triazolo[1,5-a]pyridine
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6-Bromo-[1,2,4]triazolo[4,3-a]pyridine-3-carboxylic acid
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8-Bromo-[1,2,4]triazolo[4,3-a]pyridine
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6-Bromo-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one
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Methyl 2-bromo-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylate
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Ethyl 7-bromo-[1,2,4]triazolo[1,5-a]pyridine-2-carboxylate
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8-Bromo-[1,2,4]triazolo[4,3-a]pyridine-3-carboxylic acid
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5-Bromo-[1,2,3]triazolo[1,5-a]pyridine
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8-Bromo-5-methyl-[1,2,4]triazolo[4,3-a]pyridine
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6-Bromo-3H-[1,2,3]triazolo[4,5-b]pyridine
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7-Bromo-3-methyl-[1,2,4]triazolo[4,3-a]pyridine
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8-Bromo-3-methyl-[1,2,4]triazolo[4,3-a]pyridine
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7-Bromo-2-methyl-[1,2,4]triazolo[1,5-a]pyridine
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6-Bromo-8-fluoro-[1,2,4]triazolo[4,3-a]pyridine-3(2H)-thione
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6-Bromo-2-phenyl-[1,2,4]triazolo[1,5-a]pyridine
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8-Bromo-[1,2,4]triazolo[4,3-a]pyridine-6-carboxylic acid
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tert-Butyl 4-(6-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-yl)piperidine-1-carboxylate
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2-Bromo-8-phenyl-[1,2,4]triazolo[1,5-a]pyridine