406911-89-5

Basic information

• Product Name: 2,7-Benzodioxecin-1,8-dione,3,6-dihydro-(9CI)
• Synonyms: 2,7-Benzodioxecin-1,8-dione,3,6-dihydro-(9CI)
• CAS NO: 406911-89-5
• Molecular Formula: C₁₂H₁₀O₄
• Molecular Weight: 218.2054
• Product Categories: PHENYL
• Mol File: 406911-89-5.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,7-Benzodioxecin-1,8-dione,3,6-dihydro-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2,7-Benzodioxecin-1,8-dione,3,6-dihydro-(9CI)(406911-89-5)
• EPA Substance Registry System: 2,7-Benzodioxecin-1,8-dione,3,6-dihydro-(9CI)(406911-89-5)

Safety Data

• Hazardous Substances Data: 406911-89-5(Hazardous Substances Data)

Usage

Heterocyclic compound

Contains a unique six-membered ring structure with oxygen atoms positioned at the 2, 7, and 6 positions

Fused heterocyclic system

Classified as a dioxecine

Pharmaceutical industry applications

Due to its unique structure and chemical properties

Biological activities

May have various biological activities

Therapeutic uses

Potential therapeutic uses

Interesting target for research and development

Due to its unique structure and potential applications

Upstream product

• 131-17-9 diallyl phthalate 

Relevant articles and documents

Synthesis and catalytic activity of a Grubbs-Hoveyda pre-catalyst having a trimeric resting state

A Grubbs-Hoveyda pre-catalyst having a trimeric resting state based on 2,4,6-trichloro-1,3,5-triazine was synthesized and the complex was characterized by NMR, HRMS and elemental analysis. The activity of this complex for ring-closing metathesis (RCM) was

Efficient ruthenium metathesis catalysts containing carborane ligands

A first generation Hoveyda-Grubbs ruthenium complex with a closo-1,2-C 2B10H11 tag has been prepared. This new catalyst was tested in ring-closing metathesis (RCM) reactions and proved to be quite efficient. In addition, t

Recycling a homogeneous catalyst through a light-controlled phase tag

(Figure Presented) A homogeneous ruthenium-carbene complex was tagged with a lightresponding nitrobenzospiropyran group to control its solubility through reversible conversion between its neutral (lipophilic) and ionic (lipophobic) states using light irradiation (see scheme; Mes = mesityl). This tagged complex has significant catalytic activity in ring-closing metathesis reactions and was recycled several times.