Nom du produit:3-ethynyl-3-methyloxetane

IUPAC Name:3-ethynyl-3-methyloxetane

CAS:1290541-27-3
Formule moléculaire:C6H8O
Pureté:95%+
Numéro de catalogue:CM106401
Poids moléculaire:96.13

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CM106401-5g in stock ǎŌǎǸ

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Détails du produit

N° CAS:1290541-27-3
Formule moléculaire:C6H8O
Point de fusion:-
Code SMILES:CC1(C#C)COC1
Densité:
Numéro de catalogue:CM106401
Poids moléculaire:96.13
Point d'ébullition:
N° Mdl:MFCD19441315
Stockage:

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Oxetanes
Oxygen heterocycles are one of the most common heterocycles in drugs and natural products. Oxetene has high polarity and is also a good acceptor for hydrogen bond, which contributes to the metabolism and chemical stability of its host molecules. When substituted for commonly used functional groups such as gem dimethyl or carbonyl, oxetane units can induce profound changes in water solubility, lipophilicity, metabolic stability and conformational preference. Four of the FDA-approved drugs contain oxetenes: Orlistat, Paclitaxel, and two of its derivatives, Docetaxel and Cabazitaxel. Currently, oxetane-containing building blocks are flourishing in medicinal chemistry and drug discovery.

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Alicyclic Heterocycles
When the ends of the chains are joined together into a ring, cyclic compounds result; such substances often are referred to as carbocyclic or alicyclic compounds. Substitution of one or more of the ring carbon atoms in the molecules of a carbocyclic compound with a heteroatom gives a heterocyclic compound.

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Product Other Information

Product Overview 3-Ethynyl-3-methyloxetane (3-EMO) is a synthetic compound that has been widely studied for its potential applications in organic synthesis, medicinal chemistry, and biochemistry. 3-EMO is a member of the oxetane family, which is a class of compounds characterized by a three-membered ring containing an oxygen atom. 
Physical Properties It is relatively low solubility in water, which can make it difficult to work with in some applications.
Chemical Properties The advantages of using 3-Ethynyl-3-methyloxetane in laboratory experiments include its low cost, its high purity, and its ease of synthesis.
Synthesis and Application In organic synthesis, 3-Ethynyl-3-methyloxetane has been used as a starting material for the synthesis of a variety of compounds, including enantiomers, polymers, and heterocyclic compounds. In medicinal chemistry, 3-Ethynyl-3-methyloxetane has been used as a starting material for the synthesis of a variety of drugs, including antibiotics, antifungals, and antivirals. In biochemistry, 3-Ethynyl-3-methyloxetane has been used as a starting material for the synthesis of a variety of enzymes, including proteases, lipases, and aminopeptidases.
Future Directions Future research on 3-Ethynyl-3-methyloxetane could focus on further elucidating its mechanism of action, developing new synthesis methods, and exploring its potential applications in organic synthesis, medicinal chemistry, and biochemistry. Additionally, further research could be conducted to explore the potential therapeutic applications of 3-Ethynyl-3-methyloxetane, including its use as an antifungal, antiviral, and antibiotic agent. Finally, research could be conducted to explore the potential applications of 3-Ethynyl-3-methyloxetane in the food industry, such as its use as a preservative or flavoring agent.