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2-Iodobiphenyl

Base Information
  • Chemical Name:2-Iodobiphenyl
  • CAS No.:64420-96-8
  • Molecular Formula:C12H4 D5 I
  • Molecular Weight:285.068
  • Hs Code.:
  • Mol file:64420-96-8.mol
2-Iodobiphenyl

Synonyms:Pentadeuterophenyl-o-jodphenyl;2-Iodobiphenyl;2-iodo-2’,3’,4’,5’,6’-d5-1,1’-biphenyl;

Suppliers and Price of 2-Iodobiphenyl
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 5 raw suppliers
Chemical Property of 2-Iodobiphenyl
Chemical Property:
  • PSA:0.00000 
  • LogP:3.95820 
Purity/Quality:

98%,99%, *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 2-Iodobiphenyl

There total 1 articles about 2-Iodobiphenyl 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:
Multi-step reaction with 2 steps
1.1: potassium carbonate; palladium diacetate / acetone; water / 65 °C / Sealed tube; Inert atmosphere
2.1: hydrogenchloride; sodium nitrite / water / 1 h / Cooling
2.2: 20 °C
With hydrogenchloride; palladium diacetate; potassium carbonate; sodium nitrite; In water; acetone;
DOI:10.1021/acs.orglett.6b01300
Guidance literature:
With palladium diacetate; sodium carbonate; In N,N-dimethyl-formamide; at 100 ℃;
DOI:10.1039/d0cc07133a
Guidance literature:
With potassium acetate; palladium diacetate; potassium hydrogencarbonate; isopropyl alcohol; In N,N-dimethyl acetamide; water; N,N-dimethyl-formamide; at 75 ℃; for 10h; Time; Overall yield = 68 %; Schlenk technique; Inert atmosphere;
DOI:10.1021/acs.orglett.6b01300
upstream raw materials:

2,3,4,5,6-pentadeuteriumbenzeneboronic acid

Downstream raw materials:

9H-fluorene

C13H6(2)H4

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