113981-41-2

Upstream product

• 2078-54-8 2,6-diisopropylphenol 

Downstream Products

• 154787-73-2 [(η3-allyl)(μ-2,6-diisopropylphenoxide)nickel]2 
• 409360-92-5 hexa(2,6-diisopropylphenolate)trinickel 
• 212558-06-0 (2,6-Pr(i)2C₆H₃O)3Sm(THF)3 
• 217174-93-1 [(η5-C5H5)TiCl(O-2,6-(CH(CH3)2)2-C6H3)(NP(C(CH3)3)3)] 
• 1141898-49-8 Sn(2,6-diisopropylphenoxide)4 
• 1100363-12-9 Yb((CH₃)3SiNCC₆H₅N(CH₂)3NCC₆H₅NSi(CH₃)3)OC₆H₃(CH(CH₃)2)2CH₃OCH₂CH₂OCH₃ 
• 1350754-47-0 C₂₅H₃₂N₂O₂ 
• 1350754-46-9 C₂₁H₃₂N₂O₂ 
• 1391921-06-4 (nacnac)V(O{2,6-iPr₂C₆H₃}) 
• 1391921-07-5 ([(2,6-iPr₂C₆H₃)NC(Me)]2CH)V(OC₆H₃-iPr₂-2,6)(4-dimethylaminopyridine) 
• 1391921-05-3 ([(2,6-ⁱPr₂C₆H₃)NC(CH₃)]₂CH)V(O(2,6-ⁱPr₂C₆H₃)) 
• 1431150-06-9 (Me₃SiNC(Ph)N(CH₂)3NC(Ph)NSiMe₃)Y[O₂,6-(iPr)2C₆H₃](DME) 
• 363-72-4 Pentafluorobenzene 

Relevant academic research and scientific papers

Double-effect anesthetic and preparation method and application thereof

The invention belongs to the technical field of medicine and particularly relates to a double-effect anesthetic and a preparation method and application thereof.The invention discloses a compound shown in the general formula (I).The compound can generate

Propofol purification

Propofol is purified by reaction of the raw 2,6-diisopropylphenol with an alkaline agent, by isolation of the alkaline metal salt and by neutralization thereof. There is thus obtained a propofol having a purity of at least 99.90%.

A NOVEL, SIMPLE METHOD FOR THE PREPARATION OF HINDERED DIPHENYL ETHERS

The displacement of the nitro group from substituted nitrobenzenes is used for the synthesis of diphenyl ethers. 1,4-Dinitrobenzene has been converted into a variety of hindered diphenyl ethers using 2,6-disubstituted phenoxides and studies show that the mechanism of formation of the ether (5a) is radical in nature.