Home Chemistry Heterocyclic Building Blocks Thiazoles 4,5,6,7-Tetrahydrobenzo[D]Thiazole
Aromatic Substitution: The benzene ring in 4,5,6,7-tetrahydrobenzo[d]thiazole can undergo electrophilic aromatic substitution reactions, such as nitration, sulfonation, halogenation, or Friedel-Crafts reactions.
Ring Opening: The thiazole ring can potentially undergo ring-opening reactions under certain conditions, such as hydrolysis or reaction with strong nucleophiles.
Reduction: The unsaturated bonds in the molecule can be reduced to saturated bonds. For example, the double bonds can be reduced to single bonds using hydrogenation or other reducing agents.
Functional Group Transformations: Various functional groups, such as halogens, amines, or carbonyl groups, can be introduced or modified on the molecule through reactions like halogenation, amidation, or acylation.
Oxidation: Oxidation reactions can be used to convert certain functional groups in the molecule, such as alcohols to ketones or aldehydes.
Cyclization: Depending on the reaction conditions and reagents, further cyclization reactions may occur within the molecule, leading to the formation of different ring systems.
Hydrogenation: The double bonds in the molecule can be selectively hydrogenated to saturate them, typically using hydrogen gas and a catalyst.
Condensation Reactions: 4,5,6,7-tetrahydrobenzo[d]thiazole can participate in condensation reactions with other compounds, leading to the formation of larger, more complex molecules.
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Ethyl 2-amino-4,5,6,7-tetrahydrobenzo[d]thiazole-4-carboxylate
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(S)-N-(2-Amino-4,5,6,7-tetrahydrobenzo[d]thiazol-6-yl)propionamide
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2-Chloro-4,5,6,7-tetrahydrobenzo[d]thiazol-6-ol
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tert-Butyl (2-bromo-4,5,6,7-tetrahydrobenzo[d]thiazol-6-yl)carbamate
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Ethyl 2-amino-4,5,6,7-tetrahydrobenzo[d]thiazole-6-carboxylate
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Ethyl 2-bromo-4,5,6,7-tetrahydrobenzo[d]thiazole-6-carboxylate
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(R)-4,5,6,7-Tetrahydro-benzothiazole-2,6-diamine
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4-Methyl-4,5,6,7-tetrahydrobenzo[d]thiazol-2-amine
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4,5,6,7-Tetrahydrobenzo[d]thiazole-2,6-diamine
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