37500-95-1

  • Product Name:3,6-Di terbutyl carbazole
  • Molecular Formula:C20H25 N
  • Purity:99%
  • Molecular Weight:279.425
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Product Details;

CasNo: 37500-95-1

Molecular Formula: C20H25 N

factory and supplier 37500-95-1 3,6-Di terbutyl carbazole in stock

  • Molecular Formula:C20H25 N
  • Molecular Weight:279.425
  • Melting Point:233-235℃ 
  • Boiling Point:424.2±14.0 °C(Predicted) 
  • PKA:17.70±0.30(Predicted) 
  • PSA:15.79000 
  • Density:1.037 
  • LogP:5.91610 

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Two highly emissive carbazole-containing...

37500-95-1 Process route

tertiary butyl chloride
507-20-0

tertiary butyl chloride

9H-carbazole
86-74-8,105184-46-1,97960-57-1

9H-carbazole

3,6-di(tert-butyl)-9H-carbazole
37500-95-1

3,6-di(tert-butyl)-9H-carbazole

Conditions
Conditions Yield
With zinc(II) chloride; In nitromethane; at 20 ℃; for 8h;
95%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 5h;
94%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 3h; Inert atmosphere; Sonication;
92%
With zinc(II) chloride; In nitromethane; for 16h; Inert atmosphere;
86%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 5h; Inert atmosphere;
85%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 5h; Inert atmosphere;
85%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 12h; Inert atmosphere;
85%
With aluminum (III) chloride; In dichloromethane; at 20 ℃; for 24h;
83%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 6h; Inert atmosphere;
81%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 5h; Inert atmosphere;
81%
With aluminum (III) chloride; In nitromethane; at 20 ℃; Inert atmosphere; Schlenk technique;
79%
With zinc(II) chloride; Inert atmosphere;
77%
In nitromethane; at 20 ℃; for 8h; Inert atmosphere;
76%
With nitromethane; zinc(II) chloride; for 15.33h; Glovebox; Inert atmosphere;
75%
With aluminum (III) chloride; In dichloromethane; at 25 ℃; for 24h;
75%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 5h; Inert atmosphere;
73%
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃; for 12h; Inert atmosphere; Schlenk technique;
70%
With zinc(II) chloride; In nitromethane; Inert atmosphere;
70%
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃; for 24h;
69%
With aluminum (III) chloride; In dichloromethane; at 20 ℃; for 16h; Inert atmosphere;
66%
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃; for 10h;
65%
With aluminum (III) chloride; In dichloromethane; at 20 ℃;
61%
With zinc(II) chloride; In nitromethane; at 20 ℃;
60.6%
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃; for 10.3333h; Cooling with ice;
60%
9H-carbazole; With zinc(II) chloride; In nitromethane; at 20 ℃; for 0.166667h;
tertiary butyl chloride; In nitromethane; for 5h;
55%
With aluminium trichloride; In dichloromethane; at 0 - 20 ℃; for 24h;
54%
With aluminum (III) chloride; at 20 ℃; for 24h;
54%
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃;
54%
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃; for 9h;
54%
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃;
54%
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃; for 24h;
54%
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃; for 24h;
51%
With aluminum (III) chloride;
50%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 6h; Inert atmosphere;
50%
With aluminium trichloride; In dichloromethane; at 20 ℃; for 16h;
47%
With zinc(II) chloride; In nitromethane; Inert atmosphere;
46%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 24h; Inert atmosphere;
45%
With aluminum (III) chloride; In chloroform; at 0 ℃; for 12h;
40%
9H-carbazole; With zinc(II) chloride; In nitromethane; at 20 ℃; Inert atmosphere;
tertiary butyl chloride; In nitromethane; at 20 ℃; for 5h;
40%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 5h; Inert atmosphere;
39%
With aluminum (III) chloride; In dichloromethane; at 20 ℃; for 48h;
37.4%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 168h; Inert atmosphere;
36%
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
35%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 20.5h;
32%
With zinc(II) chloride; In nitromethane; at 20 ℃; for 20.5h; Inert atmosphere;
32%
With zinc(II) chloride; In nitromethane; for 5h;
11%
With zinc(II) chloride; In nitromethane; for 5h;
11%
With aluminium trichloride;
With zinc(II) chloride; In nitromethane; at 40 - 50 ℃; for 5h;
With aluminium trichloride;
With aluminium trichloride; In dichloromethane;
With aluminium trichloride;
With zinc(II) chloride; In nitromethane; at 40 - 50 ℃;
With aluminum (III) chloride; at 20 ℃; for 24h;
With zinc(II) chloride;
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
With zinc(II) chloride; In nitromethane; at 20 ℃; Molecular sieve; Inert atmosphere;
64.5 mg
With N-Bromosuccinimide;
With zinc(II) chloride; In nitromethane; Inert atmosphere; Schlenk technique;
With aluminum (III) chloride; Inert atmosphere;
With aluminum (III) chloride; In dichloromethane;
With aluminum (III) chloride;
With aluminum (III) chloride; In nitromethane; at 20 ℃; for 24h;
With nitromethane; zinc(II) chloride; at 20 ℃; for 5h; Inert atmosphere;
With aluminum (III) chloride; In dichloromethane; Inert atmosphere;
With aluminum (III) chloride; In dichloromethane; at 20 ℃; for 24h;
With aluminum (III) chloride;
With aluminum (III) chloride; In dichloromethane;
With zinc(II) chloride; In nitromethane; at 20 ℃; for 5h;
With zinc(II) chloride; In nitromethane; at 20 ℃; for 5h;
With aluminum (III) chloride;
With aluminum (III) chloride; In dichloromethane; at 20 ℃; for 24h;
With aluminum (III) chloride; In chloroform; for 16h;
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃; for 24h; Inert atmosphere;
With aluminum (III) chloride; In dichloromethane; at 0 ℃; for 12h;
With zinc(II) chloride; In nitromethane; at 20 ℃;
With zinc(II) chloride; In nitromethane; at 20 ℃; for 24h;
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
9.6 g
With zinc(II) chloride; In nitromethane; at 20 ℃; for 24h;
With zinc(II) chloride; In nitromethane; dichloromethane; for 0.5h; Sonication;
2,2'-bis(acetamido)-5,5'-di-tert-butylbiphenyl

2,2'-bis(acetamido)-5,5'-di-tert-butylbiphenyl

3,6-di(tert-butyl)-9H-carbazole
37500-95-1

3,6-di(tert-butyl)-9H-carbazole

Conditions
Conditions Yield
With phosphoric acid; In diethylene glycol; at 200 ℃; for 24h;
74%

37500-95-1 Upstream products

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    1,3,6,8-tetra-tert-butyl-9H-carbazole

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    7646-85-7

    zinc(II) chloride

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    C66H64N2O2

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