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4',5'-Dimethylfluorescein

Base Information
  • Chemical Name:4',5'-Dimethylfluorescein
  • CAS No.:118797-71-0
  • Molecular Formula:C22H16O5
  • Molecular Weight:360.366
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10152241
  • Wikidata:Q83018869
  • Mol file:118797-71-0.mol
4',5'-Dimethylfluorescein

Synonyms:4',5'-dimethylfluorescein

Suppliers and Price of 4',5'-Dimethylfluorescein
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 19 raw suppliers
Chemical Property of 4',5'-Dimethylfluorescein
Chemical Property:
  • Boiling Point:607.5 °C at 760 mmHg 
  • Flash Point:220.8 °C 
  • PSA:75.99000 
  • Density:1.5 g/cm3 
  • LogP:4.28260 
  • XLogP3:4.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:0
  • Exact Mass:360.09977361
  • Heavy Atom Count:27
  • Complexity:576
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=C(C=CC2=C1OC3=C(C24C5=CC=CC=C5C(=O)O4)C=CC(=C3C)O)O
Technology Process of 4',5'-Dimethylfluorescein

There total 1 articles about 4',5'-Dimethylfluorescein 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 Zn0.95*Ti0.05O; In neat (no solvent); at 160 ℃; for 1.5h; Green chemistry;
DOI:10.1016/j.catcom.2018.11.008
Guidance literature:
Multi-step reaction with 2 steps
1: pyridine / 2.5 h / 140 °C
2: 98.2 percent / 1,3-dibromo-5,5-dimethylhydantoin; 1,1'-azobis(cyclohexanecarbonitrile); AcOH / chlorobenzene / 72 h / 40 °C
With pyridine; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; acetic acid; 1,1'-azobis(1-cyanocyclohexanenitrile); In chlorobenzene;
DOI:10.1021/ja010059l
Guidance literature:
Multi-step reaction with 4 steps
1: pyridine / 2.5 h / 140 °C
2: 98.2 percent / 1,3-dibromo-5,5-dimethylhydantoin; 1,1'-azobis(cyclohexanecarbonitrile); AcOH / chlorobenzene / 72 h / 40 °C
3: 36.7 percent / DMSO; NaHCO3 / 4 h / 150 °C
4: 27.8 percent / sodium triacetoxyborohydride; AcOH / 1,2-dichloro-ethane / 12 h / 20 °C
With pyridine; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; sodium tris(acetoxy)borohydride; sodium hydrogencarbonate; acetic acid; dimethyl sulfoxide; 1,1'-azobis(1-cyanocyclohexanenitrile); In 1,2-dichloro-ethane; chlorobenzene;
DOI:10.1021/ja010059l
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