euglobal G2

Base Information

Chemical Name:euglobal G2
CAS No.:130288-57-2
Molecular Formula:C₂₃H₃₀O₅
Molecular Weight:386.488
Hs Code.:
Mol file:130288-57-2.mol

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

Suppliers and Price of euglobal G2

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 2 raw suppliers

Chemical Property of euglobal G2

Chemical Property:

Vapor Pressure:5.87E-11mmHg at 25°C
Boiling Point:508.4°Cat760mmHg
Flash Point:170.6°C
PSA：83.83000
Density:1.203g/cm³
LogP:4.51490

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of euglobal G2

There total 13 articles about euglobal G2 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:

Reference yield:

: 7785-70-8,25766-18-1
(+)-α-pinene

: 63861-11-0
grandinol

: 130304-62-0
euglobal-G₁

: 130288-57-2
euglobal G2

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

Reference yield:

: 215163-06-7
3,5-di-(isopropoxy)phenol

: 130288-57-2
euglobal G2

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

Reference yield:

: 215163-07-8
2-hydroxy-4,6-diisopropoxybenzaldehyde

: 130288-57-2
euglobal G2

Guidance literature:: Multi-step reaction with 5 steps

1: 91.3 percent / Raney Ni / aq. ethanol / 6 h / Heating

2: 84.6 percent / TiCl₄ / CH₂Cl₂ / 0.5 h / Ambient temperature

3: 83.4 percent / TiCl₄ / CH₂Cl₂ / 48 h / Ambient temperature

4: 41.6 percent / TiCl₄ / CH₂Cl₂ / 2 h / -20 °C

5: Et₄NOTs, DDQ / nitromethane / Ambient temperature; electrolysis: fibre coated glassy carbon anode, Pt cathode, 2.2 F

With titanium tetrachloride; tetraethylammonium tosylate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; nickel; In nitromethane; ethanol; dichloromethane;
DOI:10.1039/a802306i