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C7H3IN2O2

Base Information Edit
  • Chemical Name:C7H3IN2O2
  • CAS No.:1261481-69-9
  • Molecular Formula:C7H3IN2O2
  • Molecular Weight:274.018
  • Hs Code.:2926907090
  • Mol file:1261481-69-9.mol
C<sub>7</sub>H<sub>3</sub>IN<sub>2</sub>O<sub>2</sub>

Synonyms:

Suppliers and Price of C7H3IN2O2
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
  • SynQuest Laboratories
  • 2-Iodo-3-nitrobenzonitrile 95%
  • 1 g
  • $ 216.00
  • SynQuest Laboratories
  • 2-Iodo-3-nitrobenzonitrile 95%
  • 250 mg
  • $ 80.00
  • SynQuest Laboratories
  • 2-Iodo-3-nitrobenzonitrile 95%
  • 5 g
  • $ 656.00
  • Crysdot
  • 2-Iodo-3-nitrobenzonitrile 97%
  • 5g
  • $ 698.00
  • Alichem
  • 2-Iodo-3-nitrobenzonitrile
  • 1g
  • $ 1504.90
  • Alichem
  • 2-Iodo-3-nitrobenzonitrile
  • 500mg
  • $ 855.75
  • Alichem
  • 2-Iodo-3-nitrobenzonitrile
  • 250mg
  • $ 484.80
Total 2 raw suppliers
Chemical Property of C7H3IN2O2 Edit
Chemical Property:
  • Boiling Point:338.1±37.0 °C(Predicted) 
  • Density:2.07±0.1 g/cm3(Predicted) 
Purity/Quality:

2-Iodo-3-nitrobenzonitrile 95% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of C7H3IN2O2

There total 1 articles about C7H3IN2O2 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:
2-amino-3-nitrobenzonitrile; With hydrogenchloride; sodium nitrite; In water; at 0 - 5 ℃; for 0.5h;
With potassium iodide; In water; at 5 - 20 ℃; for 4h;
DOI:10.1007/s12039-012-0325-2
Guidance literature:
With dihydrogen peroxide; sodium carbonate; In acetone; at 5 - 20 ℃; for 1h;
DOI:10.1007/s12039-012-0325-2
Guidance literature:
Multi-step reaction with 2 steps
1: dihydrogen peroxide; sodium carbonate / acetone / 1 h / 5 - 20 °C
2: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / 0.25 h / 20 °C / Inert atmosphere
With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; dihydrogen peroxide; sodium carbonate; triethylamine; In acetone; 2: |Sonogashira Cross-Coupling / 2: |Sonogashira Cross-Coupling;
DOI:10.1007/s12039-012-0325-2
upstream raw materials:

2-amino-3-nitrobenzonitrile

Downstream raw materials:

2-iodo-3-nitrobenzamide

C15H10N2O3

C16H12N2O3

C16H12N2O4

Refernces Edit
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