4342-46-5

Basic information

• Product Name: 4-Methoxycyclohexylamine
• Synonyms: 4-Methoxycyclohexylamine;CyclohexanaMine, 4-Methoxy-
• CAS NO: 4342-46-5
• Molecular Formula: C₇H₁₅NO
• Molecular Weight: 129.2001
• Mol File: 4342-46-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 174.5 °C at 760 mmHg
• Flash Point: 53.1 °C
• Appearance: /
• Density: 0.94 g/cm³
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 10.38±0.70(Predicted)
• CAS DataBase Reference: 4-Methoxycyclohexylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Methoxycyclohexylamine(4342-46-5)
• EPA Substance Registry System: 4-Methoxycyclohexylamine(4342-46-5)

Safety Data

• Hazardous Substances Data: 4342-46-5(Hazardous Substances Data)

Usage

General Description

4-Methoxycyclohexylamine is a chemical compound that belongs to the class of cyclohexylamines. It is an organic compound with the molecular formula C7H15NO. This chemical is a clear liquid at room temperature and is slightly soluble in water. It is commonly used as an intermediate in the synthesis of pharmaceuticals, agricultural chemicals, and other organic compounds. 4-Methoxycyclohexylamine is also used as a reagent in organic chemistry reactions, and it is known for its potential to react with a variety of functional groups. Additionally, it has been reported to have potential applications in medicinal chemistry, particularly in the development of new therapeutic agents. Overall, 4-Methoxycyclohexylamine is a versatile compound with a wide range of potential applications in various industries.

Upstream product

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

Downstream Products

• 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 
• 1353733-66-0 5-(3,4-dichlorophenyl)-3-(4-methoxycyclohexyl)imino-2-(2-methoxy-3-pyridyl)amino-3,5-dihydrophenazine 
• 1353740-18-7 5-(3,4-difluorophenyl)-3-(4-methoxycyclohexyl)imino-2-(2-methoxy-3-pyridyl)amino-3,5-dihydrophenazine 
• 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 

Relevant articles and documents

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.

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.

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.