79201-43-7

Usage

Uses

Used in Organic Synthesis:
1-Cycloheptylhydrazine Hydrochloride is used as a reagent for the reduction of carbonyl compounds to alcohols, which is crucial in the synthesis of various organic compounds.
Used in Deoxygenation Processes:
As a deoxygenating agent, 1-Cycloheptylhydrazine Hydrochloride is employed in the removal of dissolved oxygen from aqueous solutions, which is important in processes where oxygen can cause unwanted side reactions or degradation.
Used as a Corrosion Inhibitor:
1-Cycloheptylhydrazine Hydrochloride serves as a corrosion inhibitor, protecting metal surfaces from corrosion, which is particularly useful in industries where metal components are exposed to corrosive environments.
Used in Pharmaceutical Industry:
1-Cycloheptylhydrazine Hydrochloride has potential applications in the pharmaceutical industry, where its reducing properties may be utilized in the development of new drugs or drug delivery systems.
Used in Agrochemical Industry:
In the agrochemical sector, 1-Cycloheptylhydrazine Hydrochloride may be employed in the synthesis of agrochemicals or as a component in formulations that enhance crop protection and yield.

InChI:InChI=1/C7H16N2.ClH/c8-9-7-5-3-1-2-4-6-7;/h7,9H,1-6,8H2;1H

Upstream product

• 79201-40-4 1-tert-butoxycarbonyl-2-cycloheptylidenehydrazine 
• 502-42-1 cycloheptanone 
• 641638-68-8 N'-cycloheptyl-hydrazinecarboxylic acid tert-butyl ester 

Downstream Products

• 680187-01-3 1-(cycloheptyl)-5-(4-chlorophenyl)-4-methyl-1H-pyrazole-3-carboxylic acid ethyl ester 
• 1426534-40-8 C₂₃H₂₈N₂O 
• 1402938-53-7 C₁₉H₂₅ClN₂O₂ 

Relevant academic research and scientific papers

A variation of the Fischer indolization involving condensation of quinone monoketals and aliphatic hydrazines

A new twist: A one-pot nitrous acid free, diazonium-free, and transition-metal-free variation of the Fischer indole synthesis has been developed. Condensation of quinone monoketals and aliphatic hydrazine hydrochlorides afforded indoles via intermediate alkylaryldiazenes. This method will complement the classical Fischer indole synthesis by providing indoles in two steps from widely available phenols under mild conditions. Copyright

Synthesis, biological evaluation, and structural studies on N1 and C5 substituted cycloalkyl analogues of the pyrazole class of CB1 and CB2 ligands

A series of N1 and C5 substituted cycloalkyl and C5 4-methylphenyl analogues of the N-(piperidin-1-yl)-4-methyl-1H-pyrazole-3-carboxamide class of cannabinoid ligands were synthesized. The analogues were evaluated for CB1 and CB2 receptor binding affinities and receptor subtype selectivity. The effects of pyrazole substitution on ligand conformation and as such receptor affinities was not readily apparent; therefore, the geometries of the N1 and C5 substituents relative to the pyrazole ring were studied using high field NMR spectroscopy and systematic molecular mechanics geometry searches. An analysis of the relative ring geometries and functional group orientations provides new insight into the structural requirements of the CB1 and CB2 ligand binding pocket.