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9-O-Acetyl-4,4'-di-O-methyllariciresil

Base Information Edit
  • Chemical Name:9-O-Acetyl-4,4'-di-O-methyllariciresil
  • CAS No.:73354-15-1
  • Molecular Formula:C24H30O7
  • Molecular Weight:430.49100
  • Hs Code.:
  • Mol file:73354-15-1.mol
9-O-Acetyl-4,4'-di-O-methyllariciresil

Synonyms:

Suppliers and Price of 9-O-Acetyl-4,4'-di-O-methyllariciresil
Supply Marketing:Edit
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
  • Crysdot
  • 9-O-Acetyl-4,4'-di-O-methyllariciresinol 95+%
  • 5mg
  • $ 810.00
  • Arctom
  • 9-O-Acetyl-4,4'-di-O-methyllariciresinol
  • 5mg
  • $ 513.00
  • Arctom
  • 9-O-Acetyl-4,4'-di-O-methyllariciresinol ≥98%
  • 5mg
  • $ 371.00
Total 13 raw suppliers
Chemical Property of 9-O-Acetyl-4,4'-di-O-methyllariciresil Edit
Chemical Property:
  • Boiling Point:534.4±50.0 °C(Predicted) 
  • PSA:72.45000 
  • Density:1.145±0.06 g/cm3(Predicted) 
  • LogP:3.83050 
Purity/Quality:

98%min *data from raw suppliers

9-O-Acetyl-4,4'-di-O-methyllariciresinol 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 9-O-Acetyl-4,4'-di-O-methyllariciresil

There total 8 articles about 9-O-Acetyl-4,4'-di-O-methyllariciresil 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 iodosylbenzene; C70H50MnN2O4(1+)*F6P(1-); In dichloromethane; at -40 ℃; for 5h; Overall yield = 44 percent; Overall yield = 18.9 mg; Resolution of racemate;
DOI:10.1021/jacs.0c09636
Guidance literature:
With iodosylbenzene; C70H50MnN2O4(1+)*F6P(1-); In dichloromethane; at -40 ℃; for 5h; Overall yield = 44 percent; Overall yield = 18.9 mg; Resolution of racemate;
DOI:10.1021/jacs.0c09636
Guidance literature:
Multi-step reaction with 2 steps
1: N-Bromosuccinimide / dichloromethane
2: dmap; pyridine
With pyridine; dmap; N-Bromosuccinimide; In dichloromethane;
DOI:10.1021/jacs.0c09636
Refernces Edit
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