The chemical substance with the name "(1aR,2R,3R,3aR,7bS)-3,3',3',3a-tetramethyl-6-oxo-2,3,3a,4,6,7b-hexahydro-1aH-spiro[naphtho[1,2-b]oxirene-5,2'-oxiran]-2-yl acetate" and CAS number "62445-06-1" is a complex organic compound characterized by its unique spirocyclic structure, which incorporates both naphthalene and oxirane moieties. This compound features multiple chiral centers, contributing to its stereochemical complexity. The presence of the acetate functional group suggests potential reactivity and solubility characteristics typical of esters. Its tetramethyl substitution indicates a high degree of branching, which may influence its physical properties, such as boiling point and solubility in various solvents. The oxo group implies potential for further chemical transformations, making it of interest in synthetic organic chemistry. Overall, this compound's intricate structure and functional groups may confer specific biological activities or applications in fields such as pharmaceuticals or materials science, although detailed studies would be necessary to elucidate its full range of properties and potential uses.

(1aR,2R,3R,3aR,7bS)-3,3',3',3a-tetramethyl-6-oxo-2,3,3a,4,6,7b-hexahydro-1aH-spiro[naphtho[1,2-b]oxirene-5,2'-oxiran]-2-yl acetate

62445-06-1: The chemical substance with the name "(1aR,2R,3R,3aR,7bS)-3,3',3',3a-tetramethyl-6-oxo-2,3,3a,4,6,7b-hexahydro-1aH-spiro[naphtho[1,2-b]oxirene-5,2'-oxiran]-2-yl acetate" and CAS number "62445-06-1" is a complex organic compound characterized by its unique spirocyclic structure, which incorporates both naphthalene and oxirane moieties. This compound features multiple chiral centers, contributing to its stereochemical complexity. The presence of the acetate functional group suggests potential reactivity and solubility characteristics typical of esters. Its tetramethyl substitution indicates a high degree of branching, which may influence its physical properties, such as boiling point and solubility in various solvents. The oxo group implies potential for further chemical transformations, making it of interest in synthetic organic chemistry. Overall, this compound's intricate structure and functional groups may confer specific biological activities or applications in fields such as pharmaceuticals or materials science, although detailed studies would be necessary to elucidate its full range of properties and potential uses.

<p>Eremofortin A, a metabolite, can be isolated from Penicillium roqueforti cultures [1].</p>

CAS 62445-06-1

(1aR,2R,3R,3aR,7bS)-3,3',3',3a-tetramethyl-6-oxo-2,3,3a,4,6,7b-hexahydro-1aH-spiro[naphtho[1,2-b]oxirene-5,2'-oxiran]-2-yl acetate

Eremofortin A

Ref: TM-T73914

Eremofortin A

Ref: 7W-GL0564