53135-64-1

Usage

InChI:InChI=1/C6H10O/c1-3-5-7-6-4-2/h1H,4-6H2,2H3

Upstream product

• 71-23-8 propan-1-ol 
• 107-08-4 1-iodo-propane 
• 107-19-7 propargyl alcohol 
• 106-96-7 propargyl bromide 

Downstream Products

• 122129-57-1 1-Phenyl-ethanone O-((E)-3-propoxy-allyl)-oxime 
• 7133-11-1 1-Propyloxy-3-<1-hydroxy-cyclohexyl>-propin-(2) 

Relevant academic research and scientific papers

Hydrolysis and Alcoholysis of Esters of o-Nitrobenzenesulfonic Acid

The rate of solvolysis of esters of o-nitrobenzenesulfonic acid with water and C1-C4 alcohols is satisfactorily described by two-parametric Hammett-Taft equation with predominating effect of the electronic factor σ*. The effect of the structure of the hydrocarbon rest in the sulfonic ester group does not fit to this relationship.

Antiulcer compounds having a substituted alkynyl or quinoxaline nucleus and methods of making thereof

This invention relates to a novel compound which is useful as a drug in preventing and/or treating peptic ulcer-related diseases, to a production process thereof and to a pharmaceutical composition containing the same. Particularly, it provides a compound which has a specified substituted alkynylpyrazine nucleus or a specified substituted alkynylquinoxaline nucleus, represented by the following formula (I) STR1 wherein A is represented by the following formula (II) or (III) STR2 and R1 is represented by the following formula (IV), STR3 and the salts thereof, a production process thereof and a pharmaceutical composition containing the same. The inventive compound is useful as a drug in preventing and/or treating peptic ulcer-related diseases.

Alkyl Ether and Enol Ether Analogs of (Z)-5-Decenyl Acetate, a Pheromone Component of the Turnip Moth, Agrotis segetum: Probing a Proposed Bioactive Conformation for Chain-Elongated Analogs

In order to test a previous conclusion that chain-elongated analogs of (Z)-5-decenyl acetate (1), a pheromone component of the turnip moth, Agrotis segetum, adopt a loop conformation of the terminal alkyl chain in the bioactive conformation, a series of alkyl ether and enol ether analogs of 1 and (Z)-5-dodecenyl acetate (2) have been synthesized and tested using single-cell electrophysiology. In these analogs a methylene group in positions 7 and 9 of 1 and in positions 7 and 11 in 2 have been replaced by an oxygen atom in order to energetically facilitate the formation of a loop conformation in the chain-elongated analogs. The electrophysiological results in combination with molecular mechanics (MM2 and MM3) calculated conformational energies show that the activity decreases of the chain-elongated ether analogs are significantly smaller than that for 2 and that these activity decreases parallel the conformational energies for a loop formation of the terminal chains in the analogs. The results support our previous conclusion that the terminal chain of chain-elongated analogs of 1 adopts a loop conformation in their bioactive conformations.

ALLENE ETHERS FOR THE CATIONIC CYCLOPENTANNELATION

Only allene ethers having a group which is capable of departing as a stable cation participate successfully in the cationic cyclopentannelation reaction.