1262033-72-6

Upstream product

• 67372-96-7 3-isopropylsalicylaldehyde 
• 88-69-7 2-(1-methylethyl)phenol 
• 50-00-0 formaldehyd 
• 26307-50-6 4-bromo-2-isopropyl-phenol 

Downstream Products

• 1262033-68-0 N-tert-butyl-3-isopropyl-5-bromosalicylaldimine 
• 1285574-12-0 5-bromo-3-isopropyl-2-methoxybenzaldehyde 
• 1617519-25-1 C₁₀H₁₃BrO₂ 
• 1617519-27-3 C₁₀H₁₂Br₂O 
• 1617519-30-8 C₂₈H₃₈Br₂N₂O₂ 
• 1285574-23-3 3-(3-cyano-5-isopropyl-4-methoxybenzoyl)-1,1-dioxo-2,3-dihydro-1,3-benzothiazole 
• 1285574-20-0 3-(3-cyano-5-isopropyl-4-methoxybenzoyl)-2,3-dihydro-1,3-benzothiazole 
• 1285574-18-6 3-cyano-5-isopropyl-4-methoxybenzoyl chloride 
• 1285574-17-5 3-cyano-5-isopropyl-4-methoxybenzoic acid 
• 1285574-16-4 3-formyl-5-isopropyl-4-methoxybenzoic acid 
• 1285574-15-3 5-bromo-1-diethoxymethyl-3-isopropyl-2-methoxybenzene 
• 1285572-68-0 3-(3-cyano-4-hydroxy-5-isopropylbenzoyl)-1,1-dioxo-1,2-dihydro-3H-1,3-benzothiazole 

Relevant academic research and scientific papers

Iron(iii)-salan complexes catalysed highly enantioselective fluorination and hydroxylation of β-keto esters and N-Boc oxindoles

Chiral iron(iii)-salan complexes catalysed highly enantioselective α-fluorination and α-hydroxylation of β-keto esters and N-Boc oxindoles to give the corresponding products in high yields and good-to-excellent ee values under mild reaction conditions. This journal is the Partner Organisations 2014.

NOVEL PHENOL DERIVATIVE

Disclosed are a novel compound and a pharmaceutical product, each having a remarkable uricosuric effect. Specifically disclosed are: a novel phenol derivative represented by general formula (1) that is shown in FIG. 1; a pharmaceutically acceptable salt t

Synthesis, structures and ethylene polymerization behavior of half-metallocene chromium(iii) catalysts bearing salicylaldiminato ligands

A series of half-metallocene chromium(iii) complexes bearing a salicylaldiminato ligand, Cp′[2-R1-4-R2-6-(CH = NR3)C6H2O]CrCl [Cp′ = Cp (1, 5), Cp* (2, 3, 4, 6, 7, 8); R1 = Ph (1, 2, 3, 5, 6, 8), iPr (4), tBu (7); R2 = H (1, 2, 3), Br (4), NO2 (5, 6, 7, 8); R3 = iPr (1, 2, 5, 6, 7), tBu (3, 4, 8)], were synthesized. The structures of complexes 1, 3-5, 7-8 were determined by single crystal X-ray diffraction analysis. The X-ray crystallographic analysis indicates that these complexes adopt a pseudo-octahedral coordination environment with a three-legged piano stool geometry. Upon activation with a small amount of AlEt3, complexes 1-8 exhibit good to high catalytic activity for ethylene polymerization and produce ultra-high molecular weight polyethylene (PE) under mild conditions. The productivity of these complexes is relatively low when activated with AlMe 3 and AliBu3. Both the productivity of these catalyst systems and the molecular weight of the produced PE can be tuned in a broad range by changing the ligands and the AlR3 co-catalyst. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.