3388-03-2

Basic information

• Product Name: 2-(7-oxabicyclo[4.1.0]hept-3-yl)spiro[1,3-dioxane-5,3'-[7]oxabicyclo[4.1.0]heptane]
• Synonyms: 2-(7-oxabicyclo[4.1.0]hept-3-yl)spiro[1,3-dioxane-5,3'-[7]oxabicyclo[4.1.0]heptane];ARALDITECY-175;BAKELITEERL-4234;2-(3,4-EPOXYCYCLOHEXYL-5,5-SPIRO-3,4-EPOXY)CYCLOHEXANE-META-DIOXANE;2-[7-oxabicyclo[4.1.0]hept-3-yl]-Spiro[1,3-yl)-3-dioxane-5,3'-(7)oxabicyclo[4.1.0]-heptane];Spiro[1,3-dioxane-5,3'-(7)oxabicyclo[4.1.0]-heptane],2-[7-oxabicyclo[4.1.0]hept-3-yl]-;cycloaliphatic epoxy resin ERL-4234;2-(3,4-Epoxy)cyclohexyl-5,1-spiro(3,4-epoxy)cyclohexyl-m-dioxane
• CAS NO: 3388-03-2
• Molecular Formula: C₁₅H₂₂O₄
• Molecular Weight: 266.33278
• EINECS: 222-216-6
• Mol File: 3388-03-2.mol

Chemical Properties

• Boiling Point: 401.2°Cat760mmHg
• Flash Point: 153°C
• Appearance: /
• Density: 1.26g/cm³
• CAS DataBase Reference: 2-(7-oxabicyclo[4.1.0]hept-3-yl)spiro[1,3-dioxane-5,3'-[7]oxabicyclo[4.1.0]heptane](CAS DataBase Reference)
• NIST Chemistry Reference: 2-(7-oxabicyclo[4.1.0]hept-3-yl)spiro[1,3-dioxane-5,3'-[7]oxabicyclo[4.1.0]heptane](3388-03-2)
• EPA Substance Registry System: 2-(7-oxabicyclo[4.1.0]hept-3-yl)spiro[1,3-dioxane-5,3'-[7]oxabicyclo[4.1.0]heptane](3388-03-2)

Safety Data

• Hazardous Substances Data: 3388-03-2(Hazardous Substances Data)

Usage

Molecular structure

Spiro ring system, consisting of two rings sharing a single atom.

Fused ring system

Composed of oxabicyclo[4.1.0]heptane and spiro[1,3-dioxane-5,3'-[7]oxabicyclo[4.1.0]heptane.

Complexity

A complex chemical compound with a unique structure.

Potential applications

May have pharmaceutical or biological activity due to its fused ring structures.

Further research

Specific properties and uses would need to be determined through additional research and analysis.

Upstream product

• 1820-50-4 3-(3-cyclohexen-1-yl)-2,4-dioxaspiro[5.5]undec-8-ene 

Relevant articles and documents

Safe, environment-friendly and controllable synthetic process of di-epoxide

The invention relates to the field of synthesis of epoxide, and more specifically, relates to a safe, environment-friendly and controllable synthetic process of di-epoxide. The synthetic process of the di-epoxide at least comprises the following steps: mixing diolefin, carboxylic acids, basic salt and solvent, and cooling; dropwise adding a hydrogen peroxide solution for 1-12 h; standing for layering to obtain a lower layer organic phase-1, washing the organic phase-1 with a cleaning solution, and standing for layering to obtain a lower layer organic phase-2; purifying. The reaction system ofthe synthetic process is simple, environmentally friendly, safe and controllable, is low in production cost, and can meet the requirements of technical economy; the prepared di-epoxide is high in purity and yield and low in solvent content, chroma and halogen content, and is suitable for large-scale industrial production.