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Acetylresveratrol

Base Information Edit
  • Chemical Name:Acetylresveratrol
  • CAS No.:411233-11-9
  • Molecular Formula:C16H14O4
  • Molecular Weight:270.285
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70194066
  • Mol file:411233-11-9.mol
Acetylresveratrol

Synonyms:Acetylresveratrol;UNII-T07O870429;4'-O-acetyl-resveratrol;DTXSID70194066;MEMZFJTYLFBJEC-UHFFFAOYSA-N;4'-acetoxy-3,5-dihydroxystilbene

Suppliers and Price of Acetylresveratrol
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
  • American Custom Chemicals Corporation
  • ACETIC ACID-4-[2-(3,5-DIHYDROXY-PHENYL)-VINYL]-PHENYL ESTER 95.00%
  • 5MG
  • $ 499.96
Total 5 raw suppliers
Chemical Property of Acetylresveratrol Edit
Chemical Property:
  • PSA:66.76000 
  • LogP:3.19350 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:270.08920892
  • Heavy Atom Count:20
  • Complexity:334
Purity/Quality:

98% *data from raw suppliers

ACETIC ACID-4-[2-(3,5-DIHYDROXY-PHENYL)-VINYL]-PHENYL ESTER 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(=O)OC1=CC=C(C=C1)C=CC2=CC(=CC(=C2)O)O
Technology Process of Acetylresveratrol

There total 17 articles about Acetylresveratrol 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 novozyme 435 from Candida antarctica; In tert-Amyl alcohol; at 40 ℃; for 120h; regioselective reaction; Enzymatic reaction;
DOI:10.1042/BSR20171712
Guidance literature:
With dimethylsulfide; boron trifluoride diethyl etherate; In dichloromethane; for 20h; Inert atmosphere;
DOI:10.1016/j.bmcl.2013.03.046
Guidance literature:
With boron trichloride; tetra-(n-butyl)ammonium iodide; In dichloromethane; at 0 - 20 ℃; for 2h;
DOI:10.1016/j.tetlet.2008.07.087
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