cas 17205-02-6|| where to buy Ethyl 3-hydroxycyclobutanecarboxylate

Produktname:Ethyl 3-hydroxycyclobutanecarboxylate

IUPAC Name:ethyl 3-hydroxycyclobutane-1-carboxylate

: CAS：17205-02-6; Molekulare Formel：C7H12O3; Reinheit：95%+

: Katalognummer：CM101700; Molekulargewicht：144.17

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CM101700-10g	in stock	Ÿƚǆ

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Produkt-Details

: CAS-Nr.:17205-02-6; Molekulare Formel:C7H12O3; Schmelzpunkt:-; SMILES-Code:O=C(C1CC(O)C1)OCC; Dichte:1.18g/cm3

: Katalognummer:CM101700; Molekulargewicht:144.17; Siedepunkt:209°C at 760 mmHg; Mdl-Nr.:MFCD09758972; Lagerung:Store at 2-8°C.

Category Infos

: Cyclobutanes; The molecular structure of cyclobutane has four carbon atoms, and its four carbon atoms are not in the same plane, which is the folded conformation of cyclobutane. Cyclobutane itself is not of commercial or biological interest, but more complex derivatives are important in biology and biotechnology. Currently, nine FDA-approved drugs contain the cyclobutane structure. From the perspective of therapeutic areas, cyclobutyl drugs are mainly distributed in popular areas such as tumors, neurological diseases, infectious diseases, endocrine and metabolic diseases.

Column Infos

: Cyclanes; Cyclanes are secondary metabolites that can be found in plants, and are also biochemicals that can be used in medicine. Cyclanes are found in pine trees, and are used in the making of plastics. Cyclenes are found in cinnamon, and have antifungal properties.

Product Other Information

Product Overview	Ethyl 3-hydroxycyclobutanecarboxylate (EH3HCB) is an organic compound with a unique structure and properties. It has been studied for its potential applications in the fields of synthetic organic chemistry and biochemistry. EH3HCB is a cyclic ester that can be synthesized using a variety of methods. It has been used in a variety of scientific research applications, and its mechanism of action and biochemical and physiological effects have been studied.
Synthesis and Application	Ethyl 3-hydroxycyclobutanecarboxylate can be synthesized in a variety of ways. One of the most common methods is the reaction of ethyl 3-hydroxycyclobutane-1-carboxylate with sodium borohydride in the presence of a base. This reaction yields Ethyl 3-hydroxycyclobutanecarboxylate as the main product, along with a small amount of byproducts. Other methods of synthesis include the reaction of ethyl 3-hydroxycyclobutane-1-carboxylate with lithium aluminum hydride, and the reaction of ethyl 3-hydroxycyclobutane-1-carboxylate with anhydrous hydrogen chloride. Ethyl 3-hydroxycyclobutanecarboxylate has been used in a variety of scientific research applications. It has been used as a precursor in the synthesis of polyhydroxycyclobutanes, which are polymers-like compounds with a wide range of potential applications. It has also been used in the synthesis of polyhydroxycyclobutyl ethers, which are polymers with potential applications in the fields of drug delivery, tissue engineering, and biomaterials. Additionally, Ethyl 3-hydroxycyclobutanecarboxylate has been used in the synthesis of polyhydroxycyclobutyl esters, which are polymers with potential applications in drug delivery and tissue engineering.
Future Directions	There are a number of potential future directions for the use of Ethyl 3-hydroxycyclobutanecarboxylate. One potential application is in the development of new drugs and drug delivery systems. Additionally, Ethyl 3-hydroxycyclobutanecarboxylate may be useful in the development of new materials for tissue engineering and biomaterials. Additionally, Ethyl 3-hydroxycyclobutanecarboxylate may be useful in the development of new catalysts for chemical reactions, and it may be useful in the development of new polymers. Finally, Ethyl 3-hydroxycyclobutanecarboxylate may be useful in the development of new methods for the synthesis of complex organic molecules.