58775-05-6

  • Product Name2,7-Di-tert-butylfluorene
  • Molecular FormulaC21H26
  • Molecular Weight278.4
  • Purity99%
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Product Details

Quick Details

  • CasNo: 58775-05-6
  • Molecular Formula: C21H26
  • Purity: 99%

Pharmaceutical Intermediates 2,7-Di-tert-butylfluorene 58775-05-6 Powder

  • Molecular Formula:C21H26
  • Molecular Weight:278.437
  • Vapor Pressure:2.06E-05mmHg at 25°C 
  • Melting Point:121-124 °C(lit.) 
  • Refractive Index:1.556 
  • Boiling Point:372.4 °C at 760 mmHg 
  • Flash Point:194.2 °C 
  • PSA:0.00000 
  • Density:0.988 g/cm3 
  • LogP:5.85280 

2,7-Di-tert-butylfluorene(Cas 58775-05-6) Usage

Chemical Properties

white powder

Uses

It is used as an organic light emitting diode (OLED) intermediate.

General Description

2,7-Di-tert-butylfluorene can be synthesized by reacting fluorene, CS2 and FeCl3 and 2-chloro-2-methylpropane. It can also be obtained by reacting fluorene with tert-butyl chloride in the presence of FeCl3.

InChI:InChI=1/C21H26/c1-20(2,3)16-7-9-18-14(12-16)11-15-13-17(21(4,5)6)8-10-19(15)18/h7-10,12-13H,11H2,1-6H3

58775-05-6 Relevant articles

Site selectivity of [RuCp]+ complexation in cyclopenta[ def ]triphenylenes

Hoggard, Bryce R.,Larsen, Christopher B.,Lucas, Nigel T.

, p. 6200 - 6209 (2014)

A series of new cyclopenta-fused triphen...

Syntheses of Silylene-Bridged Thiophene-Fused Cyclopentadienyl ansa-Metallocene Complexes for Preparing High-Performance Supported Catalyst

Sun Mi Jeong ,Ju Yong Park ,Yong Bin Hyun ,Jun Won Baek ,Hagjun Kim ,Yeokwon Yoon ,Sangchul Chung ,Junseong Lee and Bun Yeoul Lee 

Catalysts 2022, 12(3), 283;

A solution of nBuLi in hexane (4.98 g, 2.5 M, 18.0 mmol) was added dropwise to a solution of 2,7-di-tert-butylfluorene (5.00 g, 18.0 mmol) in toluene (50 mL) at room temperature …

Cyclic Olefin Copolymer Bearing Pendant Fluorenyl Groups with High Refractive Index and Low Chromatic Dispersion

Haobo Yuan, Takumitsu Kida, Yuma Ishitobi, Ryo Tanaka, Masayuki Yamaguchi, Yuushou Nakayama, and Takeshi Shiono*

Macromolecules 2022, 55, 1, 125–132

To a 500 mL two-necked flask, 2,7-di-tert-butylfluorene (5.0 g, 18 mmol) was charged under nitrogen and dissolved in Et 2 O (200 mL). The solution was cooled to 0 C and nBuLi (2.65 …

58775-05-6 Process route

9H-fluorene
86-73-7

9H-fluorene

tertiary butyl chloride
507-20-0

tertiary butyl chloride

2,7-di-tert-butyl-9H-fluorene
58775-05-6

2,7-di-tert-butyl-9H-fluorene

Conditions
Conditions Yield
With iron(III) chloride; In carbon disulfide; at 0 - 20 ℃;
93%
With iron(III) chloride; In dichloromethane; for 1h;
76%
With iron(III) chloride; In dichloromethane; for 2.5h;
72%
With iron(III) chloride; In dichloromethane; at 0 ℃; for 3h; Inert atmosphere;
72%
With iron(III) chloride; In carbon disulfide; for 3.16667h; cooling;
70%
With iron(III) chloride; In carbon disulfide; at 0 ℃; Inert atmosphere;
70%
With aluminium trichloride;
 
With aluminium trichloride; In carbon disulfide; nitrobenzene;
 
With iron(III) chloride; In carbon disulfide; at 20 ℃; for 3h; Inert atmosphere;
 
With aluminum (III) chloride; In 1,2-dichloro-ethane; at 10 - 15 ℃; for 0.75h; Temperature;
 
9H-fluorene
86-73-7

9H-fluorene

2,6-di-tert-butyl-4-methyl-phenol
128-37-0

2,6-di-tert-butyl-4-methyl-phenol

2,7-di-tert-butyl-9H-fluorene
58775-05-6

2,7-di-tert-butyl-9H-fluorene

Conditions
Conditions Yield
With aluminium trichloride; In nitromethane; for 0.25h;
83%
aluminium trichloride; nitromethane; In nitromethane; at 10 - 15 ℃; for 0.25h;
83%

58775-05-6 Upstream products

  • 86-73-7
    86-73-7

    9H-fluorene

  • 507-20-0
    507-20-0

    tertiary butyl chloride

  • 128-37-0
    128-37-0

    2,6-di-tert-butyl-4-methyl-phenol

  • 7446-70-0
    7446-70-0

    aluminium trichloride

58775-05-6 Downstream products

  • 58775-13-6
    58775-13-6

    2,7-di-tert-butylfluorenone

  • 60758-15-8
    60758-15-8

    7-tert-Butyl-2-nitrofluorene

  • 91611-99-3
    91611-99-3

    2,7-di-t-butyl-4-nitrofluorene

  • 162024-88-6
    162024-88-6

    2,7‐di‐tert‐butyl‐9‐(cyclopentadienyldiphenylmethyl)‐9H‐fluorene

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