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Chemical Structure| 50874-27-6 Chemical Structure| 50874-27-6

Structure of 50874-27-6

Chemical Structure| 50874-27-6

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Product Details of [ 50874-27-6 ]

CAS No. :50874-27-6
Formula : C10H12Br2O2
M.W : 324.01
SMILES Code : COC1=C(CBr)C=C(OC)C(CBr)=C1
MDL No. :MFCD00027922

Safety of [ 50874-27-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P264-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P403+P233-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 50874-27-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 50874-27-6 ]

[ 50874-27-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 50874-27-6 ]
  • [ 7310-97-6 ]
YieldReaction ConditionsOperation in experiment
34% 2,5-Dimethoxy-1,4-benzenedicarboxaldehyde (2) A mixture of hexamethylenetetramine (12.60 g, 90 mmol), 1 (9.72 g, 30 mmol) and CHCl3 (200 mL) was heated under reflux for 3.5 h, the solvent was evaporated under reduced pressure and 50% acetic acid (200 mL) was added to the residue, heated under reflux for 4.5 h, then concentrated hydrochloric acid (10 mL) was added to the mixture, cooled to room temperature, extracted with CHCl3 and dried with anhydrous sodium sulfate. after the solvent was evaporated under reduced pressure and the residue was recrystallized from ethyl alcohol to give bright yellow needle crystals (1.98 g, 34.0%). m.p. = 202-203 C (Lit. m.p. = 201 C [32] ); 1H NMR (500 MHz, CDCl3) delta: 10.52 (s, 2H), 7.47 (s, 2H), 3.96 (s, 6H); FT-IR (KBr) v/cm-1: 3047, 2985, 2953, 2870, 1679, 1483, 1411, 1396, 1301, 1214, 1130, 1027, 878, 660.
With sodium hydrogencarbonate; dimethyl sulfoxide; at 115℃; [00328] FIG. 33 illustrates the synthetic pathway to create DPB A-TPE. [00329] To demonstrate the potential of AIE dots for cellular and mitochondria dual targeted image-guided PDT, we synthesized a new AIEgen, DPBA-TPE (FIG. 33). 3,3'-(2,5- Dimethoxy-l,4-phenylene)bis(2-(4-bromophenyl)acrylonitrile) (5) was prepared by Knoevenagel reaction from 2,5-dimethoxybenzene-l ,4-dicarboxaldehyde (3) and bromophenylacetonitrile (4) under basic conditions. The final product was obtained with satisfactory yields by intermediate (5) and aryl amine (10) in the presence of palladium catalyst under basic conditions.
 

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