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Glabrachromene II

Base Information
  • Chemical Name:Glabrachromene II
  • CAS No.:51848-09-0
  • Molecular Formula:C21H18O5
  • Molecular Weight:350.3646
  • Hs Code.:
  • Nikkaji Number:J1.180.330J,J1.176.644G
  • Wikidata:Q76386894
  • Metabolomics Workbench ID:26584
  • ChEMBL ID:CHEMBL3581071
Glabrachromene II

Synonyms:Glabrachromene II;Glabrachromene-II;51848-09-0;CHEMBL3581071;LMPK12120108;(E)-1-(2,2-Dimethyl-5-hydroxy-2H-1-benzopyran-6-yl)-3-(1,3-benzodioxole-5-yl)-2-propene-1-one;1-(2,2-Dimethyl-5-hydroxy-2H-1-benzopyran-6-yl)-3-(1,3-benzodioxole-5-yl)-2-propene-1-one;2-Propen-1-one, 3-(1,3-benzodioxol-5-yl)-1-(5-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-, (2E)-

Suppliers and Price of Glabrachromene II
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
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Total 0 raw suppliers
Chemical Property of Glabrachromene II
Chemical Property:
  • Vapor Pressure:1.39E-12mmHg at 25°C 
  • Boiling Point:547.2°Cat760mmHg 
  • Flash Point:196.5°C 
  • Density:1.302g/cm3 
  • XLogP3:4.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:3
  • Exact Mass:350.11542367
  • Heavy Atom Count:26
  • Complexity:595
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC4=C(C=C3)OCO4)C
  • Isomeric SMILES:CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)/C=C/C3=CC4=C(C=C3)OCO4)C
Technology Process of Glabrachromene II

There total 11 articles about Glabrachromene II 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 potassium hydroxide; In ethanol; water; at 25 ℃; for 36h;
DOI:10.1080/00397919908085964
Guidance literature:
With hydrogenchloride; In methanol; for 0.25h; Heating;
Guidance literature:
2,4-Dihydroxy-3-C-prenylacetophenone; With polystyrene-based selenenyl bromide resin; In dichloromethane; at 0 - 25 ℃; for 0.333333h;
piperonal; With sodium methylate; In tetrahydrofuran; methanol; at 25 ℃; for 72h;
With dihydrogen peroxide; In tetrahydrofuran; at 25 ℃; for 0.333333h; Further stages.;
DOI:10.1021/ja002033k
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