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euglobal G1

Base Information
  • Chemical Name:euglobal G1
  • CAS No.:130304-62-0
  • Molecular Formula:C23H30O5
  • Molecular Weight:386.488
  • Hs Code.:
  • Mol file:130304-62-0.mol
euglobal G1

Synonyms:2,4-Methano-1H-xanthene-7-carboxaldehyde,2,3,4,4a,9,9a-hexahydro-6,8-dihydroxy-3,3,4a-trimethyl-5-(3-methyl-1-oxobutyl)-,(2a,4a,4ab,9ab)-(+)-; Euglobal G 1

Suppliers and Price of euglobal G1
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
  • American Custom Chemicals Corporation
  • EUGLOBAL G1 95.00%
  • 5MG
  • $ 504.13
Total 1 raw suppliers
Chemical Property of euglobal G1
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:511.8°Cat760mmHg 
  • PKA:5.58±0.60(Predicted) 
  • Flash Point:172°C 
  • PSA:83.83000 
  • Density:1.203g/cm3 
  • LogP:4.51490 
Purity/Quality:

EUGLOBAL G1 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of euglobal G1

There total 13 articles about euglobal G1 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 2,3-dicyano-5,6-dichloro-p-benzoquinone; In nitromethane; at 50 ℃; for 2h;
DOI:10.1016/j.bmc.2005.10.027
Guidance literature:
With tetraethylammonium tosylate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In nitromethane; Yield given. Yields of byproduct given; Ambient temperature; electrolysis: fibre coated glassy carbon anode, Pt cathode, 2.2 F;
DOI:10.1039/a802306i
Guidance literature:
Multi-step reaction with 6 steps
1: 88.2 percent / BF3*Et2O / 0.08 h / -10 °C
2: 91.3 percent / Raney Ni / aq. ethanol / 6 h / Heating
3: 84.6 percent / TiCl4 / CH2Cl2 / 0.5 h / Ambient temperature
4: 83.4 percent / TiCl4 / CH2Cl2 / 48 h / Ambient temperature
5: 41.6 percent / TiCl4 / CH2Cl2 / 2 h / -20 °C
6: Et4NOTs, DDQ / nitromethane / Ambient temperature; electrolysis: fibre coated glassy carbon anode, Pt cathode, 2.2 F
With boron trifluoride diethyl etherate; titanium tetrachloride; tetraethylammonium tosylate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; nickel; In nitromethane; ethanol; dichloromethane;
DOI:10.1039/a802306i
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