5240-36-8

Usage

Uses

Used in Chemical Industry:
Cyclohexane, 1-ethynyl-1-methoxyis used as a solvent for various chemical reactions due to its unique properties and ability to dissolve a wide range of substances.
Used in Pharmaceutical Production:
Cyclohexane, 1-ethynyl-1-methoxyis used as an intermediate in the synthesis of certain pharmaceuticals, contributing to the development of new drugs and medications.
Used in Plastics Manufacturing:
Cyclohexane, 1-ethynyl-1-methoxyis used in the production of plastics, where its unique properties can enhance the performance and characteristics of the final plastic products.
Further research and studies are needed to explore the full potential and implications of Cyclohexane, 1-ethynyl-1-methoxyin various industries.

Upstream product

• 67-56-1 methanol 
• 6209-75-2 1-ethynyl-1-chlorocyclohexane 
• 78-27-3 1-Ethynylcyclohexan-1-ol 
• 77-78-1 dimethyl sulfate 
• 61699-43-2 methyl 1,1-pentamethyleneprop-2-ynyl carbonate 
• 74-88-4 methyl iodide 

Downstream Products

• 84022-44-6 3-(1-Methoxy-cyclohexyl)-1-phenyl-propynone 
• 132609-14-4 3-(1-Methoxy-cyclohexyl)-1-(4-nitro-phenyl)-propynone 
• 134750-10-0 4-(1-hydroxycyclopentyl)-2-(1-methoxycyclohexyl)-3-methylene-1-butene 
• 161834-52-2 1-(6-Bromo-1-hexynyl)-1-methoxycyclohexane 
• 161834-53-3 1-(7-Bromo-1-heptynyl)-1-methoxycyclohexane 
• 161834-54-4 1-(8-Bromo-1-octynyl)-1-methoxycyclohexane 
• 184697-36-7 2-bromo-7-(1-methoxycyclohexyl)-1-hepten-6-yne 
• 15174-91-1 1-(1-methoxycyclohexyl)ethan-1-one 
• 192658-24-5 C₁₆H₂₂N₂O₃ 
• 192658-26-7 C₁₆H₂₁ClN₂O₃ 
• 170954-20-8 1-anilino-4,4-dimethyl-1-(1-methoxycyclohexyl)-1-penten-3-one 
• 1398771-36-2 (E)-2-(2-(1-methoxycyclohexyl)prop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 118804-15-2 ((1-methoxycyclohexyl)ethynyl)trimethylsilane 
• 141562-01-8 4-(1-methoxycyclohexyl)-1,1,1-trifluorobut-3-yn-2-one 

Relevant academic research and scientific papers

Gold(I)-catalyzed decarboxylation of propargyl carbonates: Reactivity reversal of the gold catalyst from π-Lewis acidity to σ-Lewis acidity

A cationic gold(I)-catalyzed decarboxylative etherification of propargyl carbonates to selectively produce propargyl ethers is reported. In the reaction the gold(I) catalyst shows a distinct σ-Lewis acidity rather than the commonly observed π-Lewis acidity, and thus catalyzes the decarboxylation of a variety of propargyl carbonates to give the corresponding propargyl ethers with high selectivity. This reaction represents a rare example of the tunable reactivity of cationic gold(I) complexes between σ-Lewis acidity and π-Lewis acidity.

THIAZOLYL-DIHYDRO-QUINAZOLINE

Disclosed are thiazolyl-dihydro-quinazolines of general formula (I) wherein the groups R1 to R4 have the meanings given in the claims and specification, the isomers thereof, and processes for preparing these compounds and their use as pharmaceutical compositions.

Synthesis and First Molecular Structure of a Bis-2-spiro-1-boraadamantane Derivative

(Matrix presented) A new method for synthesizing the 2-spiro- boraadamantane pyridine complex (2) from 1-ethynylcyclohexylmethyl ether has been developed. The chemistry has been applied to the synthesis of bis-2-spiro-1-boraadamantane-pyridine (1) from tr