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Ammiol

Base Information
  • Chemical Name:Ammiol
  • CAS No.:668-10-0
  • Molecular Formula:C14H12O6
  • Molecular Weight:276.246
  • Hs Code.:
  • UNII:6R2E7CX8FG
  • DSSTox Substance ID:DTXSID10216918
  • Nikkaji Number:J109.680J
  • Wikipedia:Ammiol
  • Wikidata:Q4747251
  • Mol file:668-10-0.mol
Ammiol

Synonyms:Ammiol;6R2E7CX8FG;UNII-6R2E7CX8FG;668-10-0;5H-Furo(3,2-g)(1)benzopyran-5-one, 7-(hydroxymethyl)-4,9-dimethoxy-;DTXSID10216918;7-(Hydroxymethyl)-4,9-dimethoxy-5H-furo(3,2-g)(1)benzopyran-5-one;C14H12O6;5H-Furo[3,2-g][1]benzopyran-5-one, 7-(hydroxymethyl)-4,9-dimethoxy-;SCHEMBL10885786;DTXCID40139409;Q4747251;7-(Hydroxymethyl)-4,9-dimethoxy-5H-furo[3,2-g]chromen-5-one #

Suppliers and Price of Ammiol
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 1 raw suppliers
Chemical Property of Ammiol
Chemical Property:
  • Vapor Pressure:5.77E-11mmHg at 25°C 
  • Boiling Point:503.7°C at 760 mmHg 
  • Flash Point:258.4°C 
  • PSA:82.04000 
  • Density:1.391g/cm3 
  • LogP:2.04870 
  • XLogP3:1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:3
  • Exact Mass:276.06338810
  • Heavy Atom Count:20
  • Complexity:420
Purity/Quality:

85.0-99.8% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C2C(=O)C=C(OC2=C(C3=C1C=CO3)OC)CO
Technology Process of Ammiol

There total 8 articles about Ammiol 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 aluminum isopropoxide; In isopropyl alcohol; for 0.25h; Heating;
DOI:10.1021/jo00200a002
Guidance literature:
With KO2; In dimethyl sulfoxide; for 0.5h; Ambient temperature;
DOI:10.1021/jo00200a002
Guidance literature:
Multi-step reaction with 3 steps
1: 1) NaOMe; 2) HCl gas / 1) toluene, reflux, 15h 2) 1 min (comparable yield with NaH instead of NaOMe)
2: 79 percent / CH3I / CH2Cl2 / 72 h / Heating
3: 27 percent / KO2 / dimethylsulfoxide / 0.5 h / Ambient temperature
With hydrogenchloride; sodium methylate; methyl iodide; In dichloromethane; dimethyl sulfoxide;
DOI:10.1021/jo00200a002
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