1073-61-6

Usage

Uses

Used in Pesticide Production:
Cyclohexane, (2-chloroethyl)is used as a key component in the production of insecticides, herbicides, and fungicides. Its chemical properties make it suitable for creating effective agents that protect crops and control pests.
Used in Organic Synthesis as a Solvent:
In the field of organic synthesis, Cyclohexane, (2-chloroethyl)serves as a solvent, facilitating various chemical reactions. Its ability to dissolve a range of substances makes it a valuable asset in this industry.
Used in Pharmaceutical Production as a Chemical Intermediate:
Cyclohexane, (2-chloroethyl)is utilized as a chemical intermediate in the production of pharmaceuticals. Its role in the synthesis of certain drugs highlights its importance in the development of new medications.
Used in Dye Production as a Chemical Intermediate:
Similarly, in the dye industry, Cyclohexane, (2-chloroethyl)is employed as a chemical intermediate, contributing to the creation of various dyes used in different applications.
Given the compound's classification as a hazardous substance, it is crucial to implement proper safety measures during its production, use, and disposal to minimize potential health and environmental impacts.

Upstream product

• 4442-79-9 cyclohexylethan-1-ol 

Downstream Products

• 201286-79-5 1-(2-Cyclohexyl-ethyl)-3-methyl-1H-indole-6-carboxylic acid methyl ester 
• 1310572-11-2 5,5'''-di(2-cyclohexyl-ethyl)-[2,2';5',2'';5'',2''']-quaterthiophene 
• 1310572-15-6 2-(2-cyclohexyl-ethyl)-thiophene 

Relevant academic research and scientific papers

Correlation of Alkyl and Polar Groups in the Gas-Phase Pyrolysis Kinetics of β-Substituted Ethyl Chloride

The gas-phase pyrolysis kinetics of several β-alkyl-substituted ethyl chlorides were studied in a static system over the temperature range of 400.1-470.1 deg C and a pressure range of 32-317 torr.The reactions in seasoned vessels, with the radical chain i

H-aggregation strategy in the design of molecular semiconductors for highly reliable organic thin film transistors

Four new quaterthiophene derivatives with end-groups composed of dicyclohexyl ethyl (DCE4T), dicyclohexyl butyl (DCB4T), cyclohexyl ethyl (CE4T), and cyclohexyl butyl (CB4T) were designed. All materials showed high solubility in common organic solvents. UV-vis absorption measurements showed that the quaterthiophene derivatives with asymmetrically substituted cyclohexyl end-groups (CE4T and CB4T) preferred H-type aggregation whereas those with symmetrically substituted cyclohexyl end-groups (DCE4T and DCB4T) preferred J-type aggregation. The molecular structure-dependent packing (H or J) of the new quaterthiophene derivatives was analyzed by grazing-incidence wide-angle X-ray scattering (GIWAXS) measurements. The field-effect mobilities of devices that incorporated the asymmetrical molecules, CE4T and CB4T, were quite high, above 10 - 2 cm 2 V - 1 s - 1 , due to H-aggregation, whereas the field-effect mobilities of devices that incorporated symmetrical molecules, DCE4T and DCB4T, were poor, below 10 - 4 cm 2 V - 1 s - 1 , due to J-aggregation. More importantly, H-aggregation within the thin film provided stable crystalline morphologies in the spin-coated films, and, thus, thin film transistors (TFTs) using cyclohexylated quaterthiophenes yielded highly reproducible transistor performances. The distributions of measured field-effect mobilities in transistors based on cyclohexylated quaterthiophenes with H-aggregation were remarkably narrow.