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1H-Indene, 5-ethyl-2,3-dihydro-

Base Information
  • Chemical Name:1H-Indene, 5-ethyl-2,3-dihydro-
  • CAS No.:52689-24-4
  • Molecular Formula:C11H14
  • Molecular Weight:146.232
  • Hs Code.:2902909090
  • Mol file:52689-24-4.mol
1H-Indene, 5-ethyl-2,3-dihydro-

Synonyms:1H-Indene,5-ethyl-2,3-dihydro;

Suppliers and Price of 1H-Indene, 5-ethyl-2,3-dihydro-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 4 raw suppliers
Chemical Property of 1H-Indene, 5-ethyl-2,3-dihydro-
Chemical Property:
  • Vapor Pressure:0.158mmHg at 25°C 
  • Boiling Point:221.5°Cat760mmHg 
  • Flash Point:86.1°C 
  • PSA:0.00000 
  • Density:0.966g/cm3 
  • LogP:2.73770 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 1H-Indene, 5-ethyl-2,3-dihydro-

There total 17 articles about 1H-Indene, 5-ethyl-2,3-dihydro- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With hydrogen; platinum(IV) oxide; In tetrahydrofuran; under 1034.3 Torr; Yield given;
DOI:10.1021/jo00196a024
Guidance literature:
Multi-step reaction with 6 steps
1: thionyl chloride
2: 91 percent / AlCl3 / CS2
3: 89 percent / NaBH4 / ethanol / 25 °C
4: 97 percent / p-toluenesulfonic acid * H2O / benzene / Heating
5: 96 percent / NiCl22 / diethyl ether / Heating
6: H2 / PtO2 / tetrahydrofuran / 1034.3 Torr
With sodium tetrahydroborate; aluminium trichloride; thionyl chloride; [nickel(II)dichloride(1,3-bis(diphenylphosphino)propane)]; hydrogen; toluene-4-sulfonic acid; platinum(IV) oxide; In tetrahydrofuran; carbon disulfide; diethyl ether; ethanol; benzene;
DOI:10.1021/jo00196a024
Guidance literature:
Multi-step reaction with 8 steps
1: 95 percent / KOH / acetic acid; H2O; tetrahydrofuran
2: 85 percent / 165 °C
3: thionyl chloride
4: 91 percent / AlCl3 / CS2
5: 89 percent / NaBH4 / ethanol / 25 °C
6: 97 percent / p-toluenesulfonic acid * H2O / benzene / Heating
7: 96 percent / NiCl22 / diethyl ether / Heating
8: H2 / PtO2 / tetrahydrofuran / 1034.3 Torr
With potassium hydroxide; sodium tetrahydroborate; aluminium trichloride; thionyl chloride; [nickel(II)dichloride(1,3-bis(diphenylphosphino)propane)]; hydrogen; toluene-4-sulfonic acid; platinum(IV) oxide; In tetrahydrofuran; carbon disulfide; diethyl ether; ethanol; water; acetic acid; benzene;
DOI:10.1021/jo00196a024
upstream raw materials:

propene

INDANE

ethene

1-indan-5-yl-ethanone

Downstream raw materials:

1,2,4-benzene tricarboxylic acid

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