71650-76-5

Upstream product

• 67935-39-1 α-chloro-p-fluorobenzyl acetate 
• 352-34-1 4-fluoro-1-iodobenzene 
• 74-86-2 acetylene 
• 459-57-4 4-fluorobenzaldehyde 
• 542-92-7 cyclopenta-1,3-diene 

Downstream Products

• 1026651-07-9 7-(4-Fluoro-benzylidene)-2,3-diaza-bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid diethyl ester 
• 207856-65-3 7-(4-fluorophenylmethylene)-2,3-diazabicyclo[2.2.1]hept-2-ene 
• 207856-55-1 7-(4-Fluoro-benzylidene)-2,3-diaza-bicyclo[2.2.1]heptane-2,3-dicarboxylic acid diethyl ester 
• 1577229-50-5 C₂₄H₂₀Cl₂F₂Nb 
• 1450765-97-5 methyl (3aR,3bS,4R,5R,7S,7aS,8R,8aR)-7-(4-bromophenyl)-4-(4-fluorophenyl)-2-methyl-1,3-dioxo-2,3,3a,4,5,6,7,7a,8,8a-decahydro-1H-3b,8-ethenopyrrolo[3',4':3,4]cyclopenta[1,2-c]pyridine-5-carboxylate 

Relevant academic research and scientific papers

Reaction discovery using acetylene gas as the chemical feedstock accelerated by the stop-flow micro-tubing reactor system

Acetylene gas has been applied as a feedstock under transition-metal catalysis and photo-redox conditions to produce important chemicals including terminal alkynes, fulvenes, and fluorinated styrene compounds. The reaction discovery process was accelerated through the use of stop-flow micro-tubing reactors. This reactor prototype was developed by joining elements from both continuous micro-flow and conventional batch reactors, which was convenient and effective for gas/liquid reaction screening. Notably, the developed transformations were either inefficient or unsuccessful in conventional batch reactors. Its success relies on the unique advantages provided by this stop-flow micro-tubing reactor system.

Modified cyclopentadienyl molybdenum compounds with enhanced cytotoxic activity towards MOLT-4 leukaemia cells

A series of new cyclopentadienyl molybdenum compounds bearing substituted phenanthroline ligands [(η5-C5H4CH2C6H4X-4)Mo(CO)2(N,NL)][BF4] (X?=?F, Cl, Br; su

Ring-functionalized niobocene complexes

A series of new ring-functionalized niobocene dichloride compounds (RCH2C5H4)2NbCl2 (R = MeOCH2, (CH2)5NCH2, 2-MeOC 6H4, 3-MeOC6

1H- and 13C-NMR Investigation of Pentafulvenes

1H- and 13C-NMR spectra of a series of 6-(p-X-phenyl)pentafulvenes 1-9 as well as of 6-R-substituted and 6,6-R1,R2-disubstituted pentafulvenes 10-23 have been analysed.It turns out that the ?-system of pentafulvenes is an attractive