2435-33-8

Basic information

• Product Name: 1a,2a,3,6,6a,7a-hexahydro-3,6-ethanonaphtho[2,3-b]oxirene-2,7-dione
• CAS NO: 2435-33-8
• Molecular Formula: C₁₂H₁₂O₃
• Molecular Weight: 204.2219
• Mol File: 2435-33-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 387.9°C at 760 mmHg
• Flash Point: 176.6°C
• Density: 1.352g/cm³
• Vapor Pressure: 3.19E-06mmHg at 25°C
• Refractive Index: 1.59
• CAS DataBase Reference: 1a,2a,3,6,6a,7a-hexahydro-3,6-ethanonaphtho[2,3-b]oxirene-2,7-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1a,2a,3,6,6a,7a-hexahydro-3,6-ethanonaphtho[2,3-b]oxirene-2,7-dione(2435-33-8)
• EPA Substance Registry System: 1a,2a,3,6,6a,7a-hexahydro-3,6-ethanonaphtho[2,3-b]oxirene-2,7-dione(2435-33-8)

Safety Data

• Hazardous Substances Data: 2435-33-8(Hazardous Substances Data)

Usage

Chemical structure

Hexahydroanthrone has a cyclic structure with a six-membered and a seven-membered ring fused together.

Applications

Hexahydroanthrone is used in the production of thermoplastic and elastomeric resins, synthesis of pharmaceuticals and agrochemicals, as a solvent, and as an intermediate in organic synthesis.

Versatility

Its unique structure and properties make it a versatile chemical for various industrial and research settings.

Functional groups

The compound contains an oxirene (epoxide) group, a carbonyl group (C=O), and a six-membered and a seven-membered ring.

Hydrogenation

The term "hexahydro" in the name suggests that the compound has undergone hydrogenation, which means it has six hydrogen atoms added to its structure.

Stability

The material does not provide information on the stability of hexahydroanthrone, but its use in various applications suggests that it is stable under certain conditions.

Reactivity

The material does not provide specific information on the reactivity of hexahydroanthrone, but its use as an intermediate in organic synthesis implies that it can participate in chemical reactions.

Physical state

The material does not specify the physical state (solid, liquid, or gas) of hexahydroanthrone, but its use as a solvent suggests that it may be in a liquid state at room temperature.

Upstream product

• 2816-25-3 endo-tricyclo[6.2.2.0^2,7]dodeca-4,9-diene-3,6-dione 

Downstream Products

• 56689-13-5 (3aR,4R,7S,7aR)-1-Oxo-1,4,7,7a-tetrahydro-4,7-ethano-indene-3a-carboxylic acid 

Relevant articles and documents

SYNTHESIS AND -CYCLOREVERSION OF CAGE KETONES

A series of pentacyclic cage ketones 2b-d having no substituent was synthesized by the photochemical -cycloaddition reaction of corresponding tricyclic dienones 1b-d.The cage ketones 2b-d underwent thermal -cycloreversion to give dienones 1b-d.The reactivities were dependent on the length of the bridge "X".