CAS 19406-00-9

methyl 2-oxotetrahydrofuran-3-carboxylate

Description:

Methyl 2-oxotetrahydrofuran-3-carboxylate, with the CAS number 19406-00-9, is an organic compound characterized by its unique structure that includes a tetrahydrofuran ring, a ketone group, and an ester functional group. This compound typically appears as a colorless to pale yellow liquid and is known for its pleasant odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic characteristics. The presence of the ester group makes it reactive in various chemical reactions, including hydrolysis and transesterification. Methyl 2-oxotetrahydrofuran-3-carboxylate is often utilized in organic synthesis, particularly in the preparation of more complex molecules, and may serve as an intermediate in pharmaceutical and agrochemical applications. Its reactivity and structural features make it a valuable compound in synthetic organic chemistry. Safety data should be consulted for handling and storage, as with any chemical substance.

Formula: C₆H₈O₄

InChI: InChI=1/C6H8O4/c1-9-5(7)4-2-3-10-6(4)8/h4H,2-3H2,1H3

SMILES: COC(=O)C1CCOC1=O

Methyl 2-oxotetrahydrofuran-3-carboxylate

CAS: 19406-00-9

Formula: C₆H₈O₄

Purity: 95%

Color and Shape: Liquid

Molecular weight: 144.1253

Ref: IN-DA00387D

Methyl 2-oxotetrahydrofuran-3-carboxylate

CAS: 19406-00-9

Methyl 2-oxotetrahydrofuran-3-carboxylate

Purity: 96%

Molecular weight: 144.13g/mol

Ref: 54-OR950450

Methyl 2-oxotetrahydrofuran-3-carboxylate

CAS: 19406-00-9

Formula: C₆H₈O₄

Purity: 95%

Molecular weight: 144.126

Ref: 10-F218217

Methyl 2-oxotetrahydrofuran-3-carboxylate

CAS: 19406-00-9

Methyl 2-oxotetrahydrofuran-3-carboxylate is a synthetic compound that activates the PI3K pathway, which is a lipid kinase. It has been shown to be potent antiproliferative in cancer cell lines and xenografts. Methyl 2-oxotetrahydrofuran-3-carboxylate has been shown to inhibit the production of phosphatidylinositol, an important intermediate in the PI3K pathway. This inhibition leads to tumor cell apoptosis by inhibiting cyclic AMP synthesis, leading to decreased protein synthesis and DNA replication. In addition, this compound may also have antitumor activity by targeting the skeleton or structure of tumor cells.

Formula: C₆H₈O₄

Purity: Min. 95%

Molecular weight: 144.13 g/mol

Ref: 3D-UAA40600