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PRATENSEIN

Base Information
  • Chemical Name:PRATENSEIN
  • CAS No.:2284-31-3
  • Molecular Formula:C16H12 O6
  • Molecular Weight:300.268
  • Hs Code.:2914509090
  • Mol file:2284-31-3.mol
PRATENSEIN

Synonyms:Isoflavone,3',5,7-trihydroxy-4'-methoxy- (7CI,8CI); 3'-Hydroxybiochanin A;4'-O-Methylorobol; Pratensein; Pratenseine

Suppliers and Price of PRATENSEIN
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
  • AvaChem
  • Pratensein
  • 5mg
  • $ 290.00
  • AvaChem
  • Pratensein
  • 1mg
  • $ 119.00
  • AvaChem
  • Pratensein
  • 20mg
  • $ 690.00
  • AvaChem
  • Pratensein
  • 10mg
  • $ 490.00
  • Arctom
  • Pratensein ≥98%
  • 5mg
  • $ 418.00
Total 19 raw suppliers
Chemical Property of PRATENSEIN
Chemical Property:
  • Vapor Pressure:6.73E-14mmHg at 25°C 
  • Melting Point:272-273° 
  • Boiling Point:576.7°Cat760mmHg 
  • Flash Point:220.3°C 
  • PSA:100.13000 
  • Density:1.512g/cm3 
  • LogP:2.58540 
Purity/Quality:

99%, *data from raw suppliers

Pratensein *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of PRATENSEIN

There total 5 articles about PRATENSEIN 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 recombinant human cytochrome P450 1A1; In phosphate buffer; at 37 ℃; pH=7.4; Further Variations:; Reagents; Enzyme kinetics; Product distribution;
DOI:10.1021/jf049418x
Guidance literature:
With (R,S)-S-adenosyl-L-methionine; In dimethyl sulfoxide; at 40 ℃; for 24h; Enzymatic reaction;
DOI:10.3390/molecules22010087
Guidance literature:
With trifluoroacetic acid; for 2h; Heating;
DOI:10.1016/S0031-9422(00)82611-4
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