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isoindigotin

Base Information
  • Chemical Name:isoindigotin
  • CAS No.:476-34-6
  • Molecular Formula:C16H10 N2 O2
  • Molecular Weight:262.268
  • Hs Code.:
  • Mol file:476-34-6.mol
isoindigotin

Synonyms:Isoindigotin(6CI); [D3,3'-Biindoline]-2,2'-dione(7CI,8CI); Indin; Isoindigo; D3,3'-Bioxindole

Suppliers and Price of isoindigotin
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
  • TRC
  • Isoindigo
  • 1g
  • $ 185.00
  • TRC
  • Isoindigo
  • 10g
  • $ 1455.00
  • Medical Isotopes, Inc.
  • Isoindigo
  • 10 g
  • $ 2200.00
  • Crysdot
  • Isoindigotin 95+%
  • 250mg
  • $ 356.00
  • Crysdot
  • Isoindigotin 95+%
  • 100mg
  • $ 223.00
  • Crysdot
  • Isoindigotin 95+%
  • 1g
  • $ 890.00
  • Chemenu
  • [3,3''-Biindolinylidene]-2,2''-dione 95%
  • 1g
  • $ 832.00
  • Aaron Chemicals
  • isoindigotin 98%
  • 200mg
  • $ 90.00
Total 26 raw suppliers
Chemical Property of isoindigotin
Chemical Property:
  • Vapor Pressure:2.79E-13mmHg at 25°C 
  • Melting Point:398 °C 
  • Boiling Point:576.3°Cat760mmHg 
  • PKA:11.36±0.20(Predicted) 
  • Flash Point:245.1°C 
  • PSA:65.18000 
  • Density:1.417g/cm3 
  • LogP:2.67180 
Purity/Quality:

97% *data from raw suppliers

Isoindigo *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Isoindigo has proven successful as an electron-accepting building block for the preparation of electroactive materials for organic electronics. Meisoindigo, as a functionalized Isoindigo, has been used as an indirubin substitute for the treatment of chronic myeloid leukemia (CML).
Technology Process of isoindigotin

There total 52 articles about isoindigotin 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 hydrogenchloride; In acetic acid; Heating;
DOI:10.1002/hlca.19880710521
Guidance literature:
With carbon oxide sulfide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In acetonitrile; at 25 ℃; for 24h; under 6000.6 Torr; Inert atmosphere; Autoclave;
Guidance literature:
With carbon oxide sulfide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In acetonitrile; at 25 ℃; for 24h; under 6000.6 Torr; Solvent; Reagent/catalyst; chemoselective reaction; Catalytic behavior; Autoclave;
DOI:10.1039/d1ob02157e
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