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Ethyl 3-bromo-4-iodobenzoate

Base Information Edit
  • Chemical Name:Ethyl 3-bromo-4-iodobenzoate
  • CAS No.:386267-31-8
  • Molecular Formula:C9H8BrIO2
  • Molecular Weight:354.96709
  • Hs Code.:
  • Mol file:386267-31-8.mol
Ethyl 3-bromo-4-iodobenzoate

Synonyms:Ethyl 3-bromo-4-iodobenzoate

Suppliers and Price of Ethyl 3-bromo-4-iodobenzoate
Supply Marketing:Edit
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
  • Matrix Scientific
  • Ethyl3-bromo-4-iodobenzoate >95%
  • 1g
  • $ 684.00
  • Crysdot
  • Ethyl3-bromo-4-iodobenzoate 97%
  • 250mg
  • $ 94.00
  • Crysdot
  • Ethyl3-bromo-4-iodobenzoate 97%
  • 1g
  • $ 280.00
  • Chemenu
  • ethyl3-bromo-4-iodobenzoate 95+%
  • 1g
  • $ 320.00
  • Chemcia Scientific
  • 3-Bromo-4-iodo-benzoicacidethylester 95%
  • 5 G
  • $ 995.00
  • Chemcia Scientific
  • 3-Bromo-4-iodo-benzoicacidethylester 95%
  • 1 G
  • $ 310.00
  • Ark Pharm
  • Ethyl3-bromo-4-iodobenzoate 97%
  • 1g
  • $ 132.00
  • AK Scientific
  • Ethyl3-bromo-4-iodobenzoate
  • 100mg
  • $ 105.00
  • Abosyn
  • Ethyl3-bromo-4-iodobenzoate 95-98%
  • 1g
  • $ 340.00
Total 10 raw suppliers
Chemical Property of Ethyl 3-bromo-4-iodobenzoate Edit
Chemical Property:
  • Boiling Point:341.4±27.0 °C(Predicted) 
  • PSA:26.30000 
  • Density:1.949±0.06 g/cm3(Predicted) 
  • LogP:3.23040 
  • Storage Temp.:2-8°C(protect from light) 
Purity/Quality:

97% *data from raw suppliers

Ethyl3-bromo-4-iodobenzoate >95% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of Ethyl 3-bromo-4-iodobenzoate

There total 3 articles about Ethyl 3-bromo-4-iodobenzoate 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:
ethyl 3-bromo-4-aminobenzoate; With hydrogenchloride; sodium nitrite; In water; at 0 - 5 ℃; for 0.5h;
With potassium iodide; In water; at 0 - 20 ℃; for 2.25h;
DOI:10.1021/jacs.6b10816
Guidance literature:
Multi-step reaction with 2 steps
1.1: 55 percent / Br2 / CH2Cl2 / 12 h / 20 °C
2.1: NaNO2; aq. HCl / 3 h / 20 °C
2.2: 63 percent / aq. KI / 12 h / 20 °C
With hydrogenchloride; bromine; sodium nitrite; In dichloromethane;
DOI:10.1055/s-2001-18066
Guidance literature:
Multi-step reaction with 2 steps
1.1: N-Bromosuccinimide / chloroform / 3 h / 0 °C / Inert atmosphere
2.1: sulfuric acid; sodium nitrite / water / 2 h / 0 °C / Inert atmosphere
2.2: 0 - 20 °C / Inert atmosphere
With N-Bromosuccinimide; sulfuric acid; sodium nitrite; In chloroform; water;
DOI:10.1002/anie.201106734
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