Chemistry Organic Building Blocks Aliphatic Cyclic Hydrocarbons (4-Pentylcyclohexyl)Benzene

(4-Pentylcyclohexyl)Benzene

These compounds have the same murcko framework: (4-pentylcyclohexyl)benzene

Nucleophilic Substitution: The amine group can act as a nucleophile in substitution reactions. It might react with alkyl halides or other electrophiles to form substituted amines.
Reductive Amination: The amine group can participate in reductive amination reactions, where it reacts with a carbonyl compound (e.g., aldehyde or ketone) in the presence of a reducing agent to form secondary or tertiary amines.
Acylation: The amine group may undergo acylation reactions with acid chlorides or anhydrides to form amides.
Reduction of the Nitrogen Atom: The nitrogen atom in the amine group can be reduced to form secondary or tertiary amines, depending on the reaction conditions.
Protonation/Deprotonation: The amine group can undergo protonation or deprotonation reactions, depending on the pH of the reaction medium.
Hoffmann Elimination: If subjected to certain conditions, such as high temperatures and the presence of base, the amine might undergo Hoffmann elimination to produce an alkene.
N-Methylation: The nitrogen atom can be methylated under specific conditions to form a quaternary ammonium salt.
Substitution in the Phenyl Rings: The phenyl rings may undergo substitution reactions, such as electrophilic aromatic substitution, depending on the reaction conditions.

Further Reading:

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((1S,4R)-4-Pentylcyclohexyl)Benzene (1-Phenylcyclobutyl)Methanamine (1-Phenylcyclopropyl)Methanamine (1-Phenylcyclopropyl)Methanol (3Ar,E)-4-((Z)-2-(2-Methylenecyclohexylidene)Ethylidene)Octahydro-1H-Indene (4-Cyclohexylphenyl)Boronic Acid (4-Pentylcyclohexyl)Benzene (4-Propylcyclohexyl)Benzene (9H-Fluoren-2-Yl)Boronic Acid (9H-Fluoren-9-Yl)Methyl (4-Methoxybenzyl)Carbamate (Cyclopropylmethoxy)Benzene 1,1-Difluorocyclobutane 1,1-Difluorocyclohexane 1,1-Difluorocyclopentane 1-Bromo-2-Cyclopropylbenzene 1-Bromo-3-Cyclopropylbenzene 1-Chloro-2-Cyclopropylbenzene 1-Cyclohexyl-2-Fluorobenzene 1-Cyclopropyl-3-Methylbenzene 1-Methylcyclohex-1-Ene 1-Phenylcyclobutan-1-Amine 1-Phenylcyclobutane-1-Carbonitrile 1-Phenylcyclobutane-1-Carboxylic Acid 1-Phenylcyclohexane-1-Carboxylic Acid 1-Phenylcyclopropan-1-Amine 1-Phenylcyclopropane-1-Carbonitrile 1-Phenylcyclopropane-1-Carboxylic Acid 2-((((9H-Fluoren-9-Yl)Methoxy)Carbonyl)Amino)-2-Phenylacetic Acid 2-Bromo-9,9-Diphenyl-9H-Fluorene 2-Bromo-9H-Fluorene 2-Cyclohexylacetic Acid 2-Cyclopropyl-4-Phenylquinoline 2-Cyclopropylpyridine 2-Cyclopropylpyrimidine 2-Iodo-9H-Fluorene 2-Methylcyclohexan-1-One 2-Phenylcyclopropan-1-Amine 3,3-Dimethylcyclohexan-1-One 3-Cyclopropylpyridine 3-Methylcyclohexan-1-One 4-Cyclohexylbenzoic Acid 4-Cyclohexylbenzonitrile 4-Cyclohexylphenol 5-Azaspiro[2.4]Heptane 6-Azaspiro[2.5]Octane 9,9-Dimethyl-9H-Fluorene Bicyclo[1.1.1]Pentan-1-Ylmethanol Bicyclo[1.1.1]Pentane-1-Carboxylic Acid Bicyclo[2.2.1]Hept-2-Ene Bicyclo[2.2.1]Heptane Bromocyclohexane Cyclobutanamine Cyclobutanecarboxylic Acid Cyclobutanol Cyclobutylmethanol Cycloheptane Cyclohex-3-Ene-1-Carboxylic Acid Cyclohexanamine Cyclohexanecarboxylic Acid Cyclohexanol Cyclohexylmethanol Cyclopentanamine Cyclopentanecarboxylic Acid Cyclopentanol Cyclopropoxybenzene Ethyl 1-Phenylcyclopropane-1-Carboxylate Ethyl 2-Phenylcyclopropane-1-Carboxylate Ethyl Cyclohexanecarboxylate Isopropylcyclohexane Methoxycyclohexane Methyl 1-Phenylcyclopropane-1-Carboxylate Methyl 4-Oxocyclohexane-1-Carboxylate Methyl Bicyclo[1.1.1]Pentane-1-Carboxylate Methyl Cyclobutanecarboxylate Methyl Cyclohexanecarboxylate Methyl Cyclopentanecarboxylate N-Methylcyclohexanamine Naphthalene-1,4-Dione Spiro[3.3]Heptane Tert-Butyl (1-Phenylcyclopropyl)Carbamate Tert-Butyl (2-Phenylcyclopropyl)Carbamate Tert-Butyl Bicyclo[1.1.1]Pentan-1-Ylcarbamate Tert-Butyl Cyclobutylcarbamate Tert-Butyl Cyclohexylcarbamate Tert-Butyl Cyclopentylcarbamate

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