97546-25-3

Basic information

• Product Name: C₂₄H₂₆O₁₁
• Synonyms: C₂₄H₂₆O₁₁
• CAS NO: 97546-25-3
• Molecular Weight: 490.464
• Mol File: 97546-25-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: C₂₄H₂₆O₁₁(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₄H₂₆O₁₁(97546-25-3)
• EPA Substance Registry System: C₂₄H₂₆O₁₁(97546-25-3)

Safety Data

• Hazardous Substances Data: 97546-25-3(Hazardous Substances Data)

Upstream product

• 85-44-9 phthalic anhydride 
• 37860-51-8 tetraethylene glycol di(p-toluenesulfonate) 
• 112-60-7 Tetraethylene glycol 

Downstream Products

• 929539-09-3 C₃₄H₄₂O₁₁ 
• 25741-33-7 Tetraethylenglykol-bis-(allylphthalat) 

Relevant articles and documents

Efficient synthesis of 19-31 membered macrocyclic tetralactones via ring closing metathesis in ionic liquids

The ring closing metathesis reaction in the presence of Grubbs catalyst was demonstrated using several ionic liquids to synthesize a range of macrocyclic tetralactones having ring size of 19 to 31 membered with different spacers. The ionic liquid [mmim][PF6] was found to be an excellent solvent and the recovery of the catalyst was demonstrated. X-ray analysis of a representative macrocyclic tetralactone was also reported.

Desymmetrization of cyclic anhydrides using dihydroxy compounds: Selective synthesis of macrocyclic tetralactones

The desymmetrization of cyclic anhydrides is carried out using dihydroxy compounds. A mild route to synthesize fused saturated/unsaturated macrocyclic tetralactones with different ring sizes (20-34) having a wide variety of spacers is described. The structure is confirmed by the representative single-crystal X-ray analysis. The multiple reduction of unsaturated macrocyclic tetralactones is also illustrated. This method is mild, selective, and efficient and achieves high yield.