4342-46-5

Usage

Uses

Used in Pharmaceutical Industry:
4-Methoxycyclohexylamine is used as an intermediate in the synthesis of various pharmaceuticals for its ability to react with a range of functional groups, contributing to the development of new therapeutic agents.
Used in Agricultural Chemicals Industry:
4-Methoxycyclohexylamine serves as an intermediate in the production of agricultural chemicals, leveraging its reactivity to create compounds that can be used in crop protection and other agricultural applications.
Used in Organic Chemistry as a Reagent:
4-Methoxycyclohexylamine is utilized as a reagent in organic chemistry reactions due to its potential to engage with multiple functional groups, facilitating the synthesis of complex organic molecules.
Used in Medicinal Chemistry for Therapeutic Agent Development:
4-Methoxycyclohexylamine is applied in medicinal chemistry for the development of new therapeutic agents, capitalizing on its versatility and reactivity to create novel treatments for various medical conditions.

Upstream product

• 51-66-1 4-methoxyacetanilide 
• 1073973-07-5 2-(4-Methoxy-cyclohexyl)-isoindole-1,3-dione 
• 104-94-9 4-methoxy-aniline 
• 616-38-6 carbonic acid dimethyl ester 
• 96-49-1 [1,3]-dioxolan-2-one 

Downstream Products

• 197786-85-9 (8β)-trans-N-(4-Methoxycyclohexyl)-1-isopropyl-6-methylergoline-8-carboxamide 
• 1033776-91-8 2-hydroxy-N-(4-methoxycyclohexyl)-2-(4-trifluoromethylphenyl)acetamide 
• 1353740-18-7 5-(3,4-difluorophenyl)-3-(4-methoxycyclohexyl)imino-2-(2-methoxy-3-pyridyl)amino-3,5-dihydrophenazine 
• 1353733-66-0 5-(3,4-dichlorophenyl)-3-(4-methoxycyclohexyl)imino-2-(2-methoxy-3-pyridyl)amino-3,5-dihydrophenazine 
• 387825-48-1 cis-8-methoxy-1,3-diazaspiro[4,5]-decane-2,4-dione 
• 387825-55-0 cis-1-amino-4-methoxycyclohexane-1-carboxylic acid 
• 753441-74-6 methyl-cis-1-amino-4-methoxy-cyclohexanecarboxylate 
• 1353734-12-9 5-(4-trifluoromethoxyphenyl)-3-(4-methoxycyclohexyl)imino-2-(2-methoxy-3-pyridyl)amino-3,5-dihydrophenazine 
• 1353736-73-8 5-(4-trifluoromethylphenyl)-3-(4-methoxycyclohexyl)imino-2-(2-methoxy-3-pyridyl)amino-3,5-dihydrophenazine 
• 1353736-62-5 5-(4-trifluoromethylphenyl)-3-(4-methoxycyclohexyl)imino-2-(6-methyl-3-pyridyl)amino-3,5-dihydrophenazine 
• 1353736-84-1 5-(4-trifluoromethylphenyl)-3-(4-methoxycyclohexyl)imino-2-(2-methyl-3-pyridyl)amino-3,5-dihydrophenazine 

Relevant academic research and scientific papers

Novel spirodecenol compound and preparation method thereof

The invention discloses a novel spirodecenol compound and a preparation method thereof, and belongs to the technical field of pesticide synthesis. The invention adopts the key point that the novel spirodecenol compound has a structure as described in the specification. The invention also discloses a novel spirodecenol compound and a preparation method thereof. According to the invention, a novel spirodecenol compound is synthesized by a new method, a reaction process is simple and easy to operate, raw materials are cheap and easy to obtain, the reaction efficiency is high, the repeatability isgood, the insecticidal activity effect is obvious, and the spirodecenol compound has a good application prospect.

Preparation method and application of novel aminoazaheterocycles compound

The invention discloses a preparation method and application of a novel aminoazaheterocycles compound, and belongs to the technical field of applied chemistry. The technical scheme disclosed by the invention is characterized in that the novel aminoazaheterocycles compound has a following structure: a formula shown in the description. The invention further discloses the preparation method of the novel aminoazaheterocycles compound. The novel aminoazaheterocycles compound is synthesized through a new method; a reaction process is simple to operate and feasible, and raw materials are cheap and easy to obtain; the reaction efficiency is relatively high, and the repeatability is relatively good; the insecticidal activity effect is obvious.

Novel triazole methyl ester compound and preparation method thereof

The invention discloses a novel triazole methyl ester compound and a preparation method thereof, and belongs to the technical field of application chemistry. The invention adopts a key point that thenovel triazole methyl ester compound has a structure as described in the specification. The invention also discloses a novel triazole methyl ester compound and a preparation method thereof. Accordingto the invention, a novel triazole methyl ester compound is synthesized by a new method, a reaction process is simple and easy to operate, raw materials are cheap and easy to obtain, the reaction efficiency is high, the repeatability is good, and the insecticidal activity effect is obvious.

Novel preparation method of spirotetramat

The invention discloses a novel preparation method of spirotetramat and belongs to the technical field of pesticide syntyesis. The key point of the technical scheme is as follows: the method is characterized by carrying out cyclization reaction via 1-amin

Ruthenium-Na2CO3-catalyzed one-pot synthesis of ring-hydrogenated carbamates from aromatic amines and organic carbonates under H2

A facile and efficient one-pot procedure for the synthesis of ring hydrogenated carbamates from aromatic amine and alkylene carbonate under H2 gas pressure has been developed using a heterogeneous catalyst system comprising ruthenium and alkali metal carbonates. The effects of temperature, H2 pressure, catalyst (types of loaded metal and their supports), molar ratio of substrate/catalyst, and solvent were also investigated. Among the alkali metal carbonates, the sodium carbonate was found as best promoter for nucleophilic attack and ring-opening (NARO) reaction and thus increased the yield of ring hydrogenated carbamate up to 88% when using Ru/C as ring hydrogenation (RH) catalyst. This catalyst system could be reused at least five times without signi?cant loss of activity, which makes this process cost-effective and eco-friendly.

A modified Curtius reaction: an efficient and simple method for direct isolation of free amine

The Curtius rearrangement and related reactions are often used to convert carboxylic acids to the corresponding primary amines. However, this reaction often requires harsh conditions for hydrolysis of the isocyanate intermediates to amines, and can also be contaminated by the formation of corresponding ureas due to the reactive nature of the intermediates. We have discovered that by quenching the isocyanate intermediates with sodium trimethylsilanolate, the free amines can be isolated after aqueous workup. This mild and fast procedure provides free amines in one pot with good yields.

Tetrahydroindole and Tetrahydroindazole Derivatives

The invention provides indole and indazole compounds of Formula (I) or pharmaceutically acceptable salts thereof which are useful for treating and/or preventing diseases and/or disorders ameliorated by the inhibition of Heat-Shock Protein 90. The invention further provides pharmaceutical compositions comprising compounds of Formula (I) and methods of preparing compounds of Formula (I).