p-(2-(Allyloxy)-6-ethyl-11,12-dihydrodibenzo(a,e)cycloocten-5-yl)phenol

Base Information

Chemical Name:p-(2-(Allyloxy)-6-ethyl-11,12-dihydrodibenzo(a,e)cycloocten-5-yl)phenol
CAS No.:85850-87-9
Molecular Formula:C₂₇H₂₆O₂
Molecular Weight:382.502
Hs Code.:
UNII:GGH4F21R3T
Nikkaji Number:J69.599H
ChEMBL ID:CHEMBL263212
Mol file:85850-87-9.mol

Synonyms:BRN 5626682;GGH4F21R3T;UNII-GGH4F21R3T;p-(2-(Allyloxy)-6-ethyl-11,12-dihydrodibenzo(a,e)cycloocten-5-yl)phenol;Phenol, p-(2-(allyloxy)-6-ethyl-11,12-dihydrodibenzo(a,e)cycloocten-5-yl)-;85850-87-9;CHEMBL263212;LS-103863;p-(2-Allyloxy-6-ethyl-11,12-dihydrodibenzo[a,e]cycloocten-5-yl)phenol;PHENOL, 4-(6-ETHYL-11,12-DIHYDRO-2-(2-PROPEN-1-YLOXY)DIBENZO(A,E)CYCLOOCTEN-5-YL)-

Suppliers and Price of p-(2-(Allyloxy)-6-ethyl-11,12-dihydrodibenzo(a,e)cycloocten-5-yl)phenol

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 3 raw suppliers

Chemical Property of p-(2-(Allyloxy)-6-ethyl-11,12-dihydrodibenzo(a,e)cycloocten-5-yl)phenol

Chemical Property:

Vapor Pressure:1.53E-12mmHg at 25°C
Boiling Point:546.2°Cat760mmHg
Flash Point:277.4°C
PSA：29.46000
Density:1.114g/cm³
LogP:6.42470
XLogP3:6.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:382.193280068
Heavy Atom Count:29
Complexity:571

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1=C(C2=C(CCC3=CC=CC=C31)C=C(C=C2)OCC=C)C4=CC=C(C=C4)O
Isomeric SMILES:CC/C/1=C(/C2=C(CCC3=CC=CC=C31)C=C(C=C2)OCC=C)\C4=CC=C(C=C4)O

Technology Process of p-(2-(Allyloxy)-6-ethyl-11,12-dihydrodibenzo(a,e)cycloocten-5-yl)phenol

There total 11 articles about p-(2-(Allyloxy)-6-ethyl-11,12-dihydrodibenzo(a,e)cycloocten-5-yl)phenol 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:

: 2-Allyloxy-6-ethyl-5-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-5,6,11,12-tetrahydro-dibenzo[a,e]cycloocten-5-ol

: 85850-87-9
4-((Z)-2-Allyloxy-6-ethyl-11,12-dihydro-dibenzo[a,e]cycloocten-5-yl)-phenol

Guidance literature:: With hydrogenchloride; In ethanol; for 1h; Yield given; Heating;
DOI:10.1021/jm00362a009

Reference yield:

: 36603-49-3
4-(tetrahydropyran-2'-yloxy)-1-bromobenzene

: 85850-87-9
4-((Z)-2-Allyloxy-6-ethyl-11,12-dihydro-dibenzo[a,e]cycloocten-5-yl)-phenol

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) BuLi / 1.) THF, -70 deg C, 1 h, 2.) THF, RT, 18 h

2: conc. HCl / ethanol / 1 h / Heating

With hydrogenchloride; n-butyllithium; In ethanol;
DOI:10.1021/jm00362a009

Reference yield:

: 17910-71-3
2-<2-(3-methoxyphenyl)ethyl>benzoic acid

: 85850-87-9
4-((Z)-2-Allyloxy-6-ethyl-11,12-dihydro-dibenzo[a,e]cycloocten-5-yl)-phenol

Guidance literature:: Multi-step reaction with 10 steps

1: LiAlH₄ / diethyl ether; tetrahydrofuran / 4 h / Heating

2: thionyl chloride / toluene / 1 h / 80 °C

3: ethanol; H₂O / 12 h / Heating

4: aq. KOH / ethanol / 3 h / Heating

5: 1.) LDA / 1.) hexane, THF, -70 deg C, 1.5 h, 2.) hexane, THF, from -70 deg C to RT

6: 55 percent / P₂O₅, MeSO₃H / 1 h / Ambient temperature

7: 90 percent / pyridine hydrochloride / 0.5 h / 210 °C

8: 93 percent / K₂CO₃ / acetone / 3 h / Heating

9: 1.) BuLi / 1.) THF, -70 deg C, 1 h, 2.) THF, RT, 18 h

10: conc. HCl / ethanol / 1 h / Heating

With hydrogenchloride; potassium hydroxide; lithium aluminium tetrahydride; n-butyllithium; thionyl chloride; methanesulfonic acid; pyridine hydrochloride; phosphorus pentoxide; potassium carbonate; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; ethanol; water; acetone; toluene;
DOI:10.1021/jm00362a009