108714-73-4

Basic information

• Product Name: 2-Amino-9,9-dimethylfluorene
• Synonyms: 9H-Fluoren-2-amine,9,9-dimethyl-;Fluoren-2-amine,9,9-dimethyl-;2-AMINO-9,9-DIMETHYLFLUORENE;9,9-Dimethyl-9H-fluoren-2-amine;2-Amino-9,9-dimethyl;2-Amino-9,9-dimethyl-9H-fluorene;9,9-DiMethyl-9H-fluoren-2-a Mine、2-AMino-9,9-diMethylfluorene;2-AMino-9,9-diMethylfluorene,9,9-diMethyl-2-AMinofluorene
• CAS NO: 108714-73-4
• Molecular Formula: C₁₅H₁₅N
• Molecular Weight: 209.29
• EINECS: 1312995-182-4
• Product Categories: Electronic Chemicals;Fluorene Series;organic chemicals and derivatives/others;OLED;OLED materials,pharm chemical,electronic
• Mol File: 108714-73-4.mol
• Article Data: 8

Chemical Properties

• Melting Point: 166.0 to 170.0 °C
• Boiling Point: 374.2 °C at 760 mmHg
• Flash Point: 194.3 °C
• Appearance: Off-white/Powder
• Density: 1.107
• Vapor Pressure: 8.46E-06mmHg at 25°C
• Refractive Index: 1.631
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 4.35±0.40(Predicted)
• CAS DataBase Reference: 2-Amino-9,9-dimethylfluorene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Amino-9,9-dimethylfluorene(108714-73-4)
• EPA Substance Registry System: 2-Amino-9,9-dimethylfluorene(108714-73-4)

Safety Data

• Hazardous Substances Data: 108714-73-4(Hazardous Substances Data)

Usage

Chemical Properties

White solid

InChI:InChI=1/C15H15N/c1-15(2)13-6-4-3-5-11(13)12-8-7-10(16)9-14(12)15/h3-9H,16H2,1-2H3

Upstream product

• 86-73-7 9H-fluorene 
• 605644-46-0 9,9-dimethyl-2-nitro-9H-indole 
• 28320-31-2 2-bromo-9,9-dimethyl-9H-fluorene 
• 4569-45-3 9,9-dimethyl-9H-fluorene 
• 63021-04-5 2-acetamido-9,9-dimethylfluorene 

Downstream Products

• 1356174-65-6 9,9-dimethyl-N-(4-phenylnaphthalen-1-yl)-9H-fluorene-2-amine 
• 1356174-59-8 C₃₇H₂₈N₂ 
• 1356174-76-9 C₄₂H₃₄N₂ 
• 897671-69-1 N?(biphenyl?4?yl)?9,9?dimethyl?9H?fluorene?2?amine 
• 1242056-42-3 N-(1,1‘-biphenyl-4-yl)-N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]-9,9-dimethyl-9H-fluoren-2-amine 

Relevant articles and documents

Photocatalytic C-H Amination of Aromatics Overcoming Redox Potential Limitations

We report the photocatalytic C-H amination of aromatics overcoming redox potential limitations. Radical cations of aromatic compounds are generated photocatalytically using Ru(phen)3(PF6)2, which has a reduction potential at a high oxidation state (Ered(RuIII/RuII) = +1.37 V vs SCE) lower than the oxidation potentials of aromatic substrates (Eox = +1.65 to +2.27 V vs SCE). The radical cations are trapped with pyridine to give N-arylpyridinium ions, which were converted to aromatic amines.

Imidazole derivatives [...] and its preparation method (by machine translation)

This invention relates to a kind of a kind of [...] imidazole derivatives and method for preparing the same. The structure of this compound is the formula is: . This method is convenient, pervasive, economic. Type I in the organic photoelectric material and based on the analysis of the fluorescence detection has a broad application prospect in the field; in addition, because of such compounds are containing two nitrogen atom heterocyclic compound, has good biological activity, can also be used as a drug intermediate, preparing human, livestock anathematic drug. (by machine translation)

Dendrimer and organic light-emitting device using the same

A dendrimer and an organic light-emitting device including an organic layer having the dendrimer.