605644-46-0

  • Product Name9,9-Dimethyl-2-nitro-9h-fluorene
  • Purity99%
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Product Details

Quick Details

  • CasNo: 605644-46-0
  • Purity: 99%

605644-46-0 Properties

  • Molecular Formula:C15H13NO2
  • Molecular Weight:239.274
  • Melting Point:100-104℃ 
  • Boiling Point:373.133 °C at 760 mmHg 
  • Flash Point:171.829 °C 
  • PSA:45.82000 
  • Density:1.205 g/cm3 
  • LogP:4.42430 

605644-46-0 Usage

Chemical Properties

Oyster solid

605644-46-0 Relevant articles

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Campbell et al.

, p. 1489,1495 (1953)

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Preparation method of 2-(4-biphenyl)amino-9,9-dimethylfluorene

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Paragraph 0017, (2019/07/04)

The invention belongs to the field of organic synthesis and provides a preparation method of a novel liquid crystal material 2-(4-biphenyl)amino-9,9-dimethylfluorene. The preparation method is characterized in that fluorene is subjected to methylation with methyl iodide to obtain 9,9-dimethylfluorene, 9,9-dimethylfluorene is subjected to nitration with nitric acid to obtain 2-nitro-9,9-dimethylfluorene, 2-nitro-9,9-dimethylfluorene is subjected to hydrazine hydrate reduction to obtain 2-amino-9,9-dimethylfluorene, and 2-amino-9,9-dimethylfluorene is subjected to reaction with bromobiphenyl toobtain 2-(4-biphenyl)-amino-9,9-dimethylfluorene; the structure of the 2-(4-biphenyl)-amino-9,9-dimethylfluorene is characterized via 1H-NMR, 13C-NMR, IR and MS. The 2-(4-biphenyl)-amino-9,9-dimethylfluorene has good thermostability and high glass transition temperature and is applicable to hole transport materials in organic light-emitting devices.

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

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Paragraph 0012; 0039, (2016/10/08)

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

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Page/Page column 25; 26; 37; 38, (2014/10/29)

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

605644-46-0 Process route

9,9-dimethyl-9H-fluorene
4569-45-3

9,9-dimethyl-9H-fluorene

9,9-dimethyl-2-nitro-9H-indole
605644-46-0

9,9-dimethyl-2-nitro-9H-indole

Conditions
Conditions Yield
With sulfuric acid; nitric acid;
74%
With nitric acid; In N,N-dimethyl-formamide; at 70 - 85 ℃; for 3h;
65%
With nitric acid; acetic acid;
With nitric acid; acetic acid; for 0.5h; Cooling with ice;
9H-fluorene
86-73-7

9H-fluorene

9,9-dimethyl-2-nitro-9H-indole
605644-46-0

9,9-dimethyl-2-nitro-9H-indole

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1.1: potassium hydroxide / dimethyl sulfoxide / 0.5 h / 20 °C
1.2: 5 h / 20 °C
2.1: acetic acid; nitric acid / 0.5 h / Cooling with ice
With nitric acid; acetic acid; potassium hydroxide; In dimethyl sulfoxide;

605644-46-0 Upstream products

  • 4569-45-3
    4569-45-3

    9,9-dimethyl-9H-fluorene

  • 86-73-7
    86-73-7

    9H-fluorene

605644-46-0 Downstream products

  • 28320-65-2
    28320-65-2

    (7-Dimethylamino-9,9-dimethyl-9H-fluoren-2-yl)-(4-dimethylamino-phenyl)-phenyl-methanol

  • 28320-64-1
    28320-64-1

    {7-[Bis-(4-dimethylamino-phenyl)-methoxy-methyl]-9,9-dimethyl-9H-fluoren-2-yl}-dimethyl-amine

  • 28320-34-5
    28320-34-5

    2-amino-7-bromo-9,9-dimethyl-9H-fluorene

  • 1268835-64-8
    1268835-64-8

    C33H26N2

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