50548-45-3

  • Product Name:1-bromodibenzo[b,d]furan
  • Molecular Formula:C12H7BrO
  • Purity:99%
  • Molecular Weight:247.091
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Product Details;

CasNo: 50548-45-3

Molecular Formula: C12H7BrO

Buy cost-effective 99% pure 1-bromodibenzo[b,d]furan 50548-45-3 now

  • Molecular Formula:C12H7BrO
  • Molecular Weight:247.091
  • Vapor Pressure:0.000136mmHg at 25°C 
  • Melting Point:67℃ 
  • Boiling Point:343.8±15.0 °C(Predicted) 
  • PSA:13.14000 
  • Density:1.577±0.06 g/cm3(Predicted) 
  • LogP:4.34850 

1-bromodibenzo[b,d]furan(Cas 50548-45-3) Usage

Synthesis

111 g (416 mmol) of 6’-bromo-2’-fluorobiphenyl-2-ol are dissolved in 21 of SeccoSolv DMF (max 0.003% of H20) and cooled to 5°C. 20 g (449 mmol) of sodium hydride (60% suspension in paraffin oil) are added in portions tothis solution, and the mixture is stirred for a further 20 mm. after the addition is complete and then heated at 100°C for 45 mm. After cooling, 500 ml of ethanol are slowly added to the mixture, which is then evaporated to dryness in a rotary evaporator and purified by chromatography. Yield: 90 g (367 mmol), 88.5% of theory.

InChI:InChI=1/C12H7BrO/c13-9-5-3-7-11-12(9)8-4-1-2-6-10(8)14-11/h1-7H

50548-45-3 Relevant articles

COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENCE DEVICE, ORGANIC ELECTROLUMINESCENCE DEVICE, AND ELECTRONIC DEVICE

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Paragraph 0265; 0272-0273, (2020/11/27)

An organic electroluminescence device ha...

COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE

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Paragraph 0341; 0345, (2020/12/25)

A compound represented by formula (1): w...

COMPOSITION FOR ORGANIC ELECTRONIC DEVICES

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Paragraph 0267-0268, (2020/08/05)

The present invention relates to a compo...

MATERIALS FOR ORGANIC ELECTROLUMINESCENT DEVICES

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Paragraph 0114; 0120, (2019/05/07)

The present invention describes amines w...

50548-45-3 Process route

6’-bromo-2’-fluoro-biphenyl-2-ol

6’-bromo-2’-fluoro-biphenyl-2-ol

1-bromodibenzo[b,d]furan
50548-45-3

1-bromodibenzo[b,d]furan

Conditions
Conditions Yield
With sodium hydride; In water; N,N-dimethyl-formamide; paraffin oil; at 5 - 100 ℃; for 1.08333h;
88.5%
With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 5 - 100 ℃; for 1.08333h;
88.5%
With sodium hydride; In N,N-dimethyl-formamide; paraffin oil; at 5 - 100 ℃; for 1.08333h;
88.5%
With sodium hydride; In water; N,N-dimethyl-formamide; paraffin oil; at 5 - 100 ℃; for 1.08333h; Inert atmosphere;
88.5%
With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 5 - 100 ℃; for 1.08333h;
88.5%
With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 5 - 100 ℃; for 1.08333h;
88.5%
With potassium carbonate; In N,N-dimethyl-formamide; at 100 ℃; for 2h; Large scale;
85%
With sodium hydride; In water; N,N-dimethyl-formamide; paraffin oil; at 5 - 100 ℃; for 1.08333h;
8.55%
1-bromodibenzo[b,d]furan-1-amine
50548-39-5

1-bromodibenzo[b,d]furan-1-amine

1-bromodibenzo[b,d]furan
50548-45-3

1-bromodibenzo[b,d]furan

Conditions
Conditions Yield
1-bromodibenzo[b,d]furan-1-amine; With sulfuric acid; In water; acetonitrile; at -5 - 15 ℃; for 0.5h; Inert atmosphere;
With isopentyl nitrite; In water; acetonitrile; at -5 - -3 ℃; for 1h;
With hypophosphorous acid; In methanol; water; acetonitrile; at -2 - 20 ℃;
61.4%
1-bromodibenzo[b,d]furan-1-amine; With sulfuric acid; In water; acetonitrile; at -5 - 15 ℃; for 0.5h; Inert atmosphere;
With isopentyl nitrite; In water; acetonitrile; at -5 - -3 ℃; for 1h;
With hypophosphorous acid; In water; acetonitrile; at -2 ℃;
61.4%
With hydrogenchloride; hypophosphoric acid; sodium nitrite;

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