3587-62-0

Basic information

• Product Name: CHLOROMETHYL CYCLOHEXYL ETHER
• Synonyms: CHLOROMETHYL CYCLOHEXYL ETHER
• CAS NO: 3587-62-0
• Molecular Formula: C₇H₁₃ClO
• Molecular Weight: 148.63052
• Mol File: 3587-62-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 185 °C
• Flash Point: 75.4°C
• Appearance: /
• Density: 1.06
• Vapor Pressure: 0.773mmHg at 25°C
• Refractive Index: 1.4650 to 1.4700
• CAS DataBase Reference: CHLOROMETHYL CYCLOHEXYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: CHLOROMETHYL CYCLOHEXYL ETHER(3587-62-0)
• EPA Substance Registry System: CHLOROMETHYL CYCLOHEXYL ETHER(3587-62-0)

Safety Data

• Hazardous Substances Data: 3587-62-0(Hazardous Substances Data)

Usage

General Description

Chloromethyl cyclohexyl ether is a chemical compound with the molecular formula C8H15ClO. It is an organic compound that is used as an intermediate in the production of pharmaceuticals and agrochemicals. It is a clear, colorless liquid with a faint odor, and it is insoluble in water but miscible with organic solvents. It is a flammable liquid and should be handled and stored with care. The primary use of chloromethyl cyclohexyl ether is as a building block in the synthesis of various organic compounds, and it is not commonly used or encountered in everyday consumer products. Due to its chemical properties and potential hazards, it should be handled by trained professionals in a controlled laboratory setting.

InChI:InChI=1/C7H13ClO/c8-6-9-7-4-2-1-3-5-7/h7H,1-6H2

Upstream product

• 1453-21-0 dicyclohexyloxymethane 
• 110-88-3 1,3,5-Trioxan 
• 108-93-0 cyclohexanol 
• 50-00-0 formaldehyd 

Downstream Products

• 92699-86-0 Cyclohexyl-(3-chlor-3-phenyl-propyl)-ether 
• 91138-97-5 <2-Chlor-propoxy>-cyclohexyloxy-methan 
• 111164-94-4 <3-Chlor-butyloxy>-cyclohexan 
• 1809-97-8 Monocyclohexyloxymethylether von Thioethylenglycol 
• 90948-71-3 <2-Chlor-ethoxy>-cyclohexyloxy-methan 
• 7706-52-7 acetic acid cyclohexyloxymethyl ester 
• 42604-09-1 (methoxymethoxy)cyclohexane 

Relevant articles and documents

Development of Acidic Imidazolium Ionic Liquids for Activation of Kraft Lignin by Controlled Oxidation: Comprehensive Evaluation and Practical Utility

A novel, eco-friendly method for the activation of lignin by controlled oxidation was studied. The results obtained for six acidic imidazolium ionic liquids containing the hydrogen sulfate anion were compared. The key goal of this research was to increase the content of carbonyl groups in the lignin structure because these may play the main role in the transport of protons and electrons in active materials for electrochemical applications. By means of a variety of analytical techniques (FTIR, 13C CP/MAS NMR, and X-ray photoelectron spectroscopy; selected reactions to determine the presence of carbonyl groups; SEM; zeta-potential analysis; thermogravimetric analysis/differential thermogravimetric analysis; and porous structure analysis), it was determined that the product obtained after treatment with 3-cyclohexyloxymethy-1-methylimidazolium hydrogen sulfate had favorable properties, in terms of the target application. Electrochemical tests proved that the obtained materials could be used as anodes in lithium batteries. The results show that the activation of lignin with ionic liquids can increase its capacity and maintain stability.

Synthesis and antibiotic activity of 1-cycloalkoxymethyl-4-dimethylaminopyridinium and 1-[(1-alkoxy)ethyl]-4-dimethylaminopyridinium chlorides

DMAP reacts readily with chloromethylcycloalkyl ethers and α-chloroethyl alkyl ethers to give stable (1a-1e) and unstable (2a-2b) pyridinium chlorides. Reaction of these chlorides with NaOH produces the corresponding 4-pyridones. All the chlorides synthesized showed antibiotic activity. Particularly high activity against microbes representing cocci, rods, fungi, and bacilli was shown by 1-cyclododecyloxymethyl-4-dimethylaminopyridinium chloride 1d and 1-[(1-dodecyloxy)ethyl]-4-dimethylaminopyridinium chloride 2f.

TRANSFORMATIONS OF DI(CYCLOHEXYLOXY)METHANE IN CHLOROFORM, INITIATED BY FREE RADICALS

Cyclohexyl formate, cyclohexane, cyclohexyl chloride, cyclohexanone and (chloromethoxy)cyclohexane are formed from di(cyclohexyloxy)methane by the action of tert-butoxyl radicals in chloroform.A scheme is proposed for the formation of the above-mentioned products through di(cyclohexyloxy)methyl and alkoxycyclohexyl radicals arising from di(cyclohexyloxy)methane.