92149-07-0

92149-07-0

92149-07-0

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1 Metric Ton

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  • Min.Order :1 Metric Ton
  • Purity: 99%
  • Payment Terms : L/C,T/T,,MoneyGram

Keywords

1,10-Phenanthroline,4,7-dimethoxy- 92149-07-0 C14H12N2O2

Quick Details

  • Appearance:solid
  • Application:Organic Chemicals
  • PackAge:as per buyers
  • ProductionCapacity:1|Metric Ton|Day
  • Storage:R.T.
  • Transportation:by courier or sea

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1.Noble Metal Catalysts (Pt.Pd...)

2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...)

3.OLED intermediates (Fluorene,Carbazole,Boric acid...)

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Details:

Product Name: 4,7-DIMETHOXY-1,10-PHENANTHROLINE, 97%
Synonyms: 4,7-DIMETHOXY-1,10-PHENANTHROLINE, 97%;4,7-Dimethoxy-1,10-phenanthroline ,98%;4,7-diMethoxyl-1,10-phenanthroline;4,7-DiMethoxy-1,10-phenanthroline 97%;[4,7-DIMETHOXY-1,10-PHENANTHROLINE, 97%];4,7-Dimethoxy-1,1-phenanthroline;4,7-dimethoxy-1,10-;4,7-Dimethoxy-1,1-phena
CAS: 92149-07-0
MF: C14H12N2O2
MW: 240.25728
EINECS:
Product Categories: Other LigandsOrganic Building Blocks;Catalysis and Inorganic Chemistry;Chemical Synthesis;Oxygen Compounds;Phenols
Mol File: 92149-07-0.mol
4,7-DIMETHOXY-1,10-PHENANTHROLINE, 97% Structure
4,7-DIMETHOXY-1,10-PHENANTHROLINE, 97% Chemical Properties
Melting point  197-212 °C
Boiling point  373.1±37.0 °C(Predicted)
density  1.25
form  Crystalline Powder
pka 6.45±0.10(Predicted)
color  White to brown
Sensitive  air sensitive
Safety Information
Hazard Codes  Xn,N
Risk Statements  22-41-50
Safety Statements  26-39-61
RIDADR  UN 3077 9/PG 3
WGK Germany  3
TSCA  No
HazardClass  9
PackingGroup  Ⅲ
HS Code  29339900
MSDS Information
4,7-DIMETHOXY-1,10-PHENANTHROLINE, 97% Usage And Synthesis
Reaction
Palladium-catalyzed synthesis of benzofurans and coumarins from phenols and olefins.
Copper-catalyzed intermolecular amidation and imidation of unactivted alkanes.
Synthesis of amides via copper-catalyzed amidation of aryl halides using isocyanides.
Copper-catalyzed benzylic C(sp3)-H alkoxylation of heterocyclic compounds.
Iridium-catalyzed silylation of aryl C-H bonds.
Palladium-catalyzed intramolecular cyclization of nitroalkenes: synthesis of thienopyrroles.
A Copper-catalyzed N-alkynylation route to 2-substitued N-alkynyl pyrroles and their cyclization into pyrrolo[2,1-c]oxazin-1-ones

 

Chemical Properties White to brown Solid
4,7-DIMETHOXY-1,10-PHENANTHROLINE, 97% Preparation Products And Raw materials
Raw materials Sodium hydroxide-->Tetrahydrofuran-->Sodium-->Phosphorus oxychloride-->Acetone-->Sodium hydride-->Sodium methanolate-->N,N-Dimethylaniline-->o-Phenylenediamine-->Diphenyl ether-->Trimethoxymethane-->2,2-Dimethyl-1,3-dioxane-4,6-dione

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