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Homopterocarpin

Base Information Edit
  • Chemical Name:Homopterocarpin
  • CAS No.:606-91-7
  • Molecular Formula:C17H16O4
  • Molecular Weight:284.312
  • Hs Code.:2932999099
  • DSSTox Substance ID:DTXSID10976040
  • Nikkaji Number:J12.284J
  • Wikidata:Q27195343
  • Metabolomics Workbench ID:133462
  • ChEMBL ID:CHEMBL396671
  • Mol file:606-91-7.mol
Homopterocarpin

Synonyms:homopterocarpin

Suppliers and Price of Homopterocarpin
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
  • Homopterocarpin 95+%
  • 5mg
  • $ 730.00
  • Arctom
  • Homopterocarpin
  • 5mg
  • $ 463.00
Total 9 raw suppliers
Chemical Property of Homopterocarpin Edit
Chemical Property:
  • Vapor Pressure:4.31E-06mmHg at 25°C 
  • Boiling Point:395°C at 760 mmHg 
  • Flash Point:140.4°C 
  • PSA:36.92000 
  • Density:1.233g/cm3 
  • LogP:3.31350 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:284.10485899
  • Heavy Atom Count:21
  • Complexity:374
Purity/Quality:

98%Min *data from raw suppliers

Homopterocarpin 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC
  • Isomeric SMILES:COC1=CC2=C(C=C1)[C@@H]3COC4=C([C@@H]3O2)C=CC(=C4)OC
Technology Process of Homopterocarpin

There total 1 articles about Homopterocarpin 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:
Multi-step reaction with 3 steps
1: 59 percent / Ti(IV)Cl4/Ti(OiPr)4 / CH2Cl2 / -78 - -25 °C
2: 87 percent / pyridine / CH2Cl2 / -70 - 20 °C
3: 92 percent / Et3NHO2CH, Pd(OAc)2, 1,1'-bis(diphenylphosphino)ferrocene / dimethylformamide / 74 °C
With pyridine; 1,1'-bis-(diphenylphosphino)ferrocene; palladium diacetate; triethylammonium formate; titanium(IV) isopropylate; titanium tetrachloride; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1039/C39890000454
Guidance literature:
Multi-step reaction with 6 steps
1: H2 / Pd-C / ethanol
2: 250 mg / Adogen 464
3: 150 mg / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / methanol / 36 h / 25 °C
4: 49 mg / NaBH4 / tetrahydrofuran; ethanol / 12 h / 25 °C
5: 52 mg / pyridine
6: 30 mg / ethyl acetate / 32 h / Irradiation
With pyridine; sodium tetrahydroborate; adogen 464; hydrogen; 2,3-dicyano-5,6-dichloro-p-benzoquinone; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; ethyl acetate;
Guidance literature:
With hydrogen; palladium on activated charcoal; In ethanol;
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