59444-49-4

Basic information

• Product Name: 1,4a,6b-trimethylhexahydro-3aH-bisoxireno[5,6:8,8a]naphtho[1,2-b]furan-2,5(1H,4aH)-dione
• CAS NO: 59444-49-4
• Molecular Formula: C₁₅H₁₈O₅
• Molecular Weight: 278.3004
• Mol File: 59444-49-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 467.4°C at 760 mmHg
• Flash Point: 278.7°C
• Density: 1.39g/cm³
• Vapor Pressure: 6.51E-09mmHg at 25°C
• Refractive Index: 1.584
• CAS DataBase Reference: 1,4a,6b-trimethylhexahydro-3aH-bisoxireno[5,6:8,8a]naphtho[1,2-b]furan-2,5(1H,4aH)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4a,6b-trimethylhexahydro-3aH-bisoxireno[5,6:8,8a]naphtho[1,2-b]furan-2,5(1H,4aH)-dione(59444-49-4)
• EPA Substance Registry System: 1,4a,6b-trimethylhexahydro-3aH-bisoxireno[5,6:8,8a]naphtho[1,2-b]furan-2,5(1H,4aH)-dione(59444-49-4)

Safety Data

• Hazardous Substances Data: 59444-49-4(Hazardous Substances Data)

Usage

Type of compound

Bicyclic organic compound

Explanation

It contains two fused rings in its structure.

Explanation

The molecule has two carbonyl groups (C=O) present.

Explanation

The presence of a bisoxireno ring, which is a six-membered ring containing two oxygen atoms.

Explanation

The presence of a naphtho ring, which is a fused benzene ring system.

Explanation

The structural features of the compound, such as the bisoxireno and naphtho rings, suggest it may have potential pharmaceutical or biological activity. However, further research and analysis are needed to determine the specific properties and potential uses.

Explanation

The compound has specific hydrogen atom positions and stereochemistry, with one hydrogen atom at the 1st position and another at the 4a position.

Explanation

The molecular formula represents the number of carbon (C), hydrogen (H), and oxygen (O) atoms in the molecule.

Explanation

The compound has a long, systematic name and a complex structure, indicating that it may have multiple functional groups and a high molecular weight.

Explanation

To fully understand the properties and potential applications of this compound, additional research and analysis are required.

Functional group

Dione

Structural feature

Trimethyl

Structural feature

Bisoxireno ring

Structural feature

Naphtho ring

Potential applications

Pharmaceutical or biological activity

Stereochemistry

1H, 4aH

Complexity

Complex chemical compound

Further research needed

Specific properties and potential uses

Upstream product

• 117152-29-1 C₁₅H₂₀O₅ 
• 423769-23-7 santonin 
• 481-06-1 santonin 
• 185432-27-3 (3S,3aS,5aS,9bS)-8-Hydroxy-3,5a,9-trimethyl-3a,4,5,5a,8,9b-hexahydro-3H-naphtho[1,2-b]furan-2-one 

Downstream Products

• 71241-93-5 isoerivanin 
• 27740-15-4 ludovicin C 
• 64929-15-3 ludovicin C 
• 71327-31-6 dehydroisoerivanin 

Relevant articles and documents

Short-step synthesis of some santanolides, dehydroisoerivanin, isoerivanin, ludovicin C, and 1α,3α-dihydroxyarbusculin B by the use of the organoselenium reduction method of epoxy ketones

Short-step synthesis of four santanolides, dehydroisoerivanin (1), isoerivanin (2), ludovicin C (3), and 1α,3α-dihydroxyarbusculin B (4) is described in which the organoselenium reduction of a cross diepoxy ketone was involved as a key step.

Modification of α-santonin. I. An abnormal chlorination of 3 hydroxy 4,5 epoxy 6,11 βH-eudesm 1 en 6,12 olide with methanesulfonyl chloride

-