CAS 19683-98-8

(3S,4R,5S)-4-Hydroxy-5-methoxy-4-[(2S,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-1-oxaspiro[2.5]octan-6-one

Description:

The chemical substance known as (3S,4R,5S)-4-Hydroxy-5-methoxy-4-[(2S,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-1-oxaspiro[2.5]octan-6-one, with the CAS number 19683-98-8, is a complex organic compound characterized by its spirocyclic structure, which includes an oxaspiro framework. This compound features multiple stereocenters, contributing to its chiral nature, and exhibits functional groups such as hydroxyl (-OH), methoxy (-OCH3), and an epoxide moiety. The presence of these functional groups suggests potential reactivity and biological activity, making it of interest in fields such as medicinal chemistry and natural product synthesis. The stereochemistry indicated by the (3S,4R,5S) and (2S,3R) descriptors is crucial for understanding its interactions and properties. Additionally, the compound's molecular structure may influence its solubility, stability, and potential applications in pharmaceuticals or agrochemicals. Overall, this substance exemplifies the complexity and diversity of organic compounds in chemical research.

Formula: C₁₆H₂₄O₅

InChI: InChI=1S/C16H24O5/c1-10(2)5-6-12-14(3,21-12)16(18)13(19-4)11(17)7-8-15(16)9-20-15/h5,12-13,18H,6-9H2,1-4H3/t12-,13-,14+,15+,16+/m1/s1

InChI key: InChIKey=NESRXFGQJARQNM-OWYFMNJBSA-N

SMILES: O[C@]1([C@@]2(CO2)CCC(=O)[C@H]1OC)[C@]3(C)[C@@H](CC=C(C)C)O3

Synonyms:

• (3R,4S,5S)-5-methoxy-4-[(3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-one
• (3S,4R,5S)-4-Hydroxy-5-methoxy-4-[(2S,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-1-oxaspiro[2.5]octan-6-one
• (3S,4R,5S)-4-hydroxy-5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-one
• (3S,4R,5S)-4-hydroxy-5-methoxy-4-[(2S)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-one
• 1-Oxaspiro[2.5]octan-6-one, 4-(1,2-epoxy-1,5-dimethyl-4-hexenyl)-4-hydroxy-5-methoxy-, (1S,2R,3S,4R,5S)-(-)-
• 1-Oxaspiro[2.5]octan-6-one, 4-hydroxy-5-methoxy-4-[(2S,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-, (3S,4R,5S)-
• 1-Oxaspiro[2.5]octan-6-one, 4-hydroxy-5-methoxy-4-[(2S,3R)-2-methyl-3-(3-methyl-2-butenyl)oxiranyl]-, (3S,4R,5S)-
• 1-Oxaspiro[2.5]octan-6-one, 4-hydroxy-5-methoxy-4-[2-methyl-3-(3-methyl-2-butenyl)oxiranyl]-, [3S-[3α,4β,4(2R*,3S*),5β]]-
• 7-Hydroxy-8-Methoxy-7-[2-Methyl-3-(3-Methylbut-2-En-1-Yl)Oxiran-2-Yl]-4-Oxaspiro[2.5]Octan-1-One
• 7-Hydroxy-8-Methoxy-7-[2-Methyl-3-(3-Methylbut-2-Enyl)Oxiran-2-Yl]-4-Oxaspiro[2.5]Octan-2-One
• Graphinone

Ovalicin

CAS: 19683-98-8

Formula: C₁₆H₂₄O₅

Purity: 99.81%

Color and Shape: Whitish. Solid

Molecular weight: 296.0

Ref: 8R-AD0081

Ovalicin-d4

CAS: 19683-98-8

Formula: C₁₆H₂₀D₄O₅

Molecular weight: 300.39

Ref: 4Z-F-113003

Ovalicin

CAS: 19683-98-8

Formula: C₁₆H₂₄O₅

Molecular weight: 296.36

Ref: 4Z-F-113002

Ovalicin

CAS: 19683-98-8

Ovalicin is a peptide that has been used in research as an activator. It is a potent and specific inhibitor of voltage-gated ion channels, such as nicotinic acetylcholine receptors. Ovalicin also interacts with other proteins, including receptor and ligand interactions, which have led to its use as a research tool for investigating protein interactions. Ovalicin can be used in pharmacology to study the effects of drugs on cells by measuring the change in ion channel activity.

Formula: C₁₆H₂₄O₅

Purity: Min. 95%

Molecular weight: 296.36 g/mol

Ref: 3D-UAA68398