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1H-INDENE,2-(2-BROMOETHYL)-2,3-DIHYDRO

Base Information
  • Chemical Name:1H-INDENE,2-(2-BROMOETHYL)-2,3-DIHYDRO
  • CAS No.:159011-42-4
  • Molecular Formula:C11H13Br
  • Molecular Weight:225.128
  • Hs Code.:
  • Mol file:159011-42-4.mol
1H-INDENE,2-(2-BROMOETHYL)-2,3-DIHYDRO

Synonyms:1H-INDENE,2-(2-BROMOETHYL)-2,3-DIHYDRO

Suppliers and Price of 1H-INDENE,2-(2-BROMOETHYL)-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
  • Labseeker
  • 1H-INDENE,2-(2-BROMOETHYL)-2,3-DIHYDRO 95
  • 25g
  • $ 3208.00
  • American Custom Chemicals Corporation
  • 1H-INDENE,2-(2-BROMOETHYL)-2,3-DIHYDRO 95.00%
  • 5MG
  • $ 505.58
Total 1 raw suppliers
Chemical Property of 1H-INDENE,2-(2-BROMOETHYL)-2,3-DIHYDRO
Chemical Property:
  • PSA:0.00000 
  • LogP:3.18640 
Purity/Quality:

1H-INDENE,2-(2-BROMOETHYL)-2,3-DIHYDRO 95 *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 1H-INDENE,2-(2-BROMOETHYL)-2,3-DIHYDRO

There total 5 articles about 1H-INDENE,2-(2-BROMOETHYL)-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 sulfuric acid; hydrogen bromide; In water; for 4h; Heating;
DOI:10.1021/jm00039a019
Guidance literature:
Multi-step reaction with 5 steps
1: 90 percent / H2SO4 / dioxane; H2O / 1 h / Heating
2: 87 percent / H2, H2SO4 / 10percent Pd/C / dioxane; H2O / 5 h / 40 - 50 °C
3: 83.3 percent / HCl(g) / 0.5 h / Heating
4: 86.4 percent / LiAlH4 / diethyl ether / 1 h / Ambient temperature
5: 74 percent / 48percent HBr, conc.H2SO4 / H2O / 4 h / Heating
With hydrogenchloride; lithium aluminium tetrahydride; sulfuric acid; hydrogen bromide; hydrogen; palladium on activated charcoal; In 1,4-dioxane; diethyl ether; water;
DOI:10.1021/jm00039a019
Guidance literature:
Multi-step reaction with 4 steps
1: 87 percent / H2, H2SO4 / 10percent Pd/C / dioxane; H2O / 5 h / 40 - 50 °C
2: 83.3 percent / HCl(g) / 0.5 h / Heating
3: 86.4 percent / LiAlH4 / diethyl ether / 1 h / Ambient temperature
4: 74 percent / 48percent HBr, conc.H2SO4 / H2O / 4 h / Heating
With hydrogenchloride; lithium aluminium tetrahydride; sulfuric acid; hydrogen bromide; hydrogen; palladium on activated charcoal; In 1,4-dioxane; diethyl ether; water;
DOI:10.1021/jm00039a019
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