Cyclopropanol, 1-ethoxy- is an organic compound characterized by its cyclopropane ring structure with an ethoxy group attached to one of the carbon atoms. This compound features a three-membered cyclopropanol ring, which contributes to its unique reactivity and strain due to the angle strain inherent in the small ring. The presence of the ethoxy group introduces an ether functional group, which can influence the compound's solubility and reactivity. Cyclopropanol derivatives are known for their potential applications in organic synthesis and as intermediates in the production of various chemicals. The compound may exhibit properties typical of both alcohols and ethers, such as hydrogen bonding capabilities and moderate volatility. Additionally, due to the strained nature of the cyclopropane ring, cyclopropanol derivatives can undergo various chemical reactions, including ring-opening reactions and rearrangements, making them interesting subjects for study in synthetic organic chemistry. Safety and handling precautions should be observed, as with many organic compounds, due to potential hazards associated with flammability and toxicity.

Cyclopropanol, 1-ethoxy-

13837-45-1: Cyclopropanol, 1-ethoxy- is an organic compound characterized by its cyclopropane ring structure with an ethoxy group attached to one of the carbon atoms. This compound features a three-membered cyclopropanol ring, which contributes to its unique reactivity and strain due to the angle strain inherent in the small ring. The presence of the ethoxy group introduces an ether functional group, which can influence the compound's solubility and reactivity. Cyclopropanol derivatives are known for their potential applications in organic synthesis and as intermediates in the production of various chemicals. The compound may exhibit properties typical of both alcohols and ethers, such as hydrogen bonding capabilities and moderate volatility. Additionally, due to the strained nature of the cyclopropane ring, cyclopropanol derivatives can undergo various chemical reactions, including ring-opening reactions and rearrangements, making them interesting subjects for study in synthetic organic chemistry. Safety and handling precautions should be observed, as with many organic compounds, due to potential hazards associated with flammability and toxicity.

<p>1-Ethoxycyclopropanol is a dehydrogenase that is activated by an acceptor, such as propionate. Its activity can be titrated and it has an acidic pH optimum. It is also a filamentous enzyme with immunocytochemical subunits. 1-Ethoxycyclopropanol has been shown to catalyze the conversion of primary alcohols to their corresponding secondary alcohols. It also has been shown to have activities against P. aeruginosa, which are bacteria that can cause lung infections in humans. This product converts alkene into secondary alcohols and also plays a role in the synthesis of amino acids.</p>

CAS 13837-45-1

Cyclopropanol, 1-ethoxy-

Cyclopropanol, 1-ethoxy-

Ref: IN-DA0018NL

1-Ethoxycyclopropanol

Ref: 3D-FE141549