• 1. Two fluorescent Schiff base sensors for Zn2+: the Zn2+/Cu2+ ion interference
  Arturo Jiménez-Sánchez,Benjamín Ortíz,Vianney Ortiz Navarrete,Norberto Farfán,Rosa Santillan Analyst 2015 140 6031

• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Secondary alcohols
• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Alcohols and polyols Secondary alcohols

Cyclohexanol,1-(aminomethyl)-, hydrochloride (1:1) and Its Significance in Modern Chemical Biology

Cyclohexanol,1-(aminomethyl)-, hydrochloride (1:1) is a compound of significant interest in the field of chemical biology, particularly due to its unique structural properties and potential applications in pharmaceutical research. This compound, identified by its CAS number 19968-85-5, has garnered attention for its role as a versatile intermediate in the synthesis of various biologically active molecules. The presence of both an amine and a hydroxyl group in its structure makes it a valuable building block for the development of novel therapeutic agents.

The chemical structure of Cyclohexanol,1-(aminomethyl)-, hydrochloride (1:1) consists of a cyclohexane ring substituted with a 1-(aminomethyl) group and a hydrochloride salt form. This configuration imparts unique reactivity and solubility characteristics, making it suitable for a wide range of applications in synthetic chemistry. The amine functionality allows for further derivatization, while the hydroxyl group can participate in hydrogen bonding interactions, enhancing the compound's bioactivity.

In recent years, there has been growing interest in the use of Cyclohexanol,1-(aminomethyl)-, hydrochloride (1:1) as a precursor in the synthesis of pharmacologically relevant molecules. Its ability to undergo various chemical transformations, such as nucleophilic substitution and condensation reactions, makes it an attractive candidate for drug discovery efforts. Researchers have leveraged its structural features to develop novel compounds with potential applications in treating various diseases.

One of the most notable areas where Cyclohexanol,1-(aminomethyl)-, hydrochloride (1:1) has shown promise is in the development of antimicrobial agents. The compound's ability to interact with biological targets has led to the synthesis of several derivatives that exhibit potent activity against bacteria and fungi. These findings have been supported by recent studies that highlight its role in disrupting microbial cell membranes and inhibiting key enzymatic pathways.

Moreover, the pharmaceutical industry has been exploring the use of Cyclohexanol,1-(aminomethyl)-, hydrochloride (1:1) in the development of central nervous system (CNS) drugs. Its structural motifs have been incorporated into molecules designed to modulate neurotransmitter activity. Preliminary studies suggest that derivatives of this compound may have therapeutic potential in treating neurological disorders such as depression and anxiety. The ability to fine-tune its pharmacological properties through structural modifications has made it a valuable scaffold for drug design.

The synthetic utility of Cyclohexanol,1-(aminomethyl)-, hydrochloride (1:1) extends beyond pharmaceutical applications. It has been utilized in the preparation of chiral auxiliaries and catalysts for asymmetric synthesis. The presence of both an amine and a hydroxyl group allows for selective functionalization, enabling chemists to construct complex molecular architectures with high precision. This has opened up new avenues for the development of enantioselective drugs and materials with tailored properties.

In conclusion, Cyclohexanol,1-(aminomethyl)-, hydrochloride (1:1), identified by CAS number 19968-85-5, is a multifaceted compound with significant implications in chemical biology and pharmaceutical research. Its unique structural features and reactivity make it an invaluable intermediate for synthesizing biologically active molecules. Recent advancements in drug discovery have highlighted its potential in developing antimicrobial agents and CNS therapeutics. As research continues to uncover new applications for this compound, its importance in modern chemical biology is likely to grow even further.

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• 24779-98-4(2-(aminomethyl)adamantan-2-ol hydrochloride)
• 37022-19-8(1-(Aminomethyl)-3-methylcyclohexanol)
• 63072-51-5(Tricyclo[4.3.1.13,8]undecan-2-ol, 2-(aminomethyl)-, hydrochloride)
• 71412-02-7(Cyclohexanol, (aminomethyl)-(6CI,9CI))
• 50361-56-3(1-(aminomethyl)cyclooctan-1-ol hydrochloride)
• 2815-39-6(1-(Aminomethyl)cycloheptanol hydrochloride)
• 911060-81-6(1-(Aminomethyl)cyclobutanol hydrochloride)
• 37022-22-3(1-(aminomethyl)-4-methylcyclohexan-1-ol)