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7-methyl-8-trifluoromethyl-10-(1'-D-ribityl)isoalloxazine

Base Information
  • Chemical Name:7-methyl-8-trifluoromethyl-10-(1'-D-ribityl)isoalloxazine
  • CAS No.:28956-72-1
  • Molecular Formula:C17H17F3N4O6
  • Molecular Weight:430.34
  • Hs Code.:
  • Mol file:28956-72-1.mol
7-methyl-8-trifluoromethyl-10-(1'-D-ribityl)isoalloxazine

Synonyms:Isoalloxazine,7-methyl-10-(D-ribo-2,3,4,5-tetrahydroxypentyl)-8-(trifluoromethyl)- (8CI);Benzo[g]pteridine, riboflavin deriv.;10-D-Ribityl-7-methyl-8-trifluoromethylisoalloxazine;7-Methyl-8-trifluoromethyl-10-(1'-D-ribityl)isoalloxazine

Suppliers and Price of 7-methyl-8-trifluoromethyl-10-(1'-D-ribityl)isoalloxazine
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 7-methyl-8-trifluoromethyl-10-(1'-D-ribityl)isoalloxazine
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:161.56000 
  • Density:1.77g/cm3 
  • LogP:-0.96480 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 7-methyl-8-trifluoromethyl-10-(1'-D-ribityl)isoalloxazine

There total 10 articles about 7-methyl-8-trifluoromethyl-10-(1'-D-ribityl)isoalloxazine 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 water; trifluoroacetic acid; at 20 ℃; for 4h;
DOI:10.1002/cbic.201200670
Guidance literature:
Multi-step reaction with 4 steps
1: hydrogen; palladium 10% on activated carbon / methanol / 2 h / Inert atmosphere
2: sodium nitrite / acetic acid / 3 h / 20 °C / Darkness
3: sodium dithionite / water; ethanol / 1.5 h / 20 °C / Inert atmosphere
4: trifluoroacetic acid; water / 4 h / 20 °C
With sodium dithionite; palladium 10% on activated carbon; water; hydrogen; trifluoroacetic acid; sodium nitrite; In methanol; ethanol; water; acetic acid;
DOI:10.1002/cbic.201200670
Guidance literature:
Multi-step reaction with 3 steps
1: sodium nitrite / acetic acid / 3 h / 20 °C / Darkness
2: sodium dithionite / water; ethanol / 1.5 h / 20 °C / Inert atmosphere
3: trifluoroacetic acid; water / 4 h / 20 °C
With sodium dithionite; water; trifluoroacetic acid; sodium nitrite; In ethanol; water; acetic acid;
DOI:10.1002/cbic.201200670
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