Retinyl phenyl ether

Base Information

Chemical Name:Retinyl phenyl ether
CAS No.:75664-68-5
Molecular Formula:C₂₆H₃₄O
Molecular Weight:362.555
Hs Code.:
Nikkaji Number:J571.784A

Synonyms:Retinyl phenyl ether;75664-68-5;15-Phenoxyretin;((3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraenyl)oxy)benzene (all-E)-;Benzene, ((3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraenyl)oxy)-, (all-E)-;Phenyl[(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)-2,4,6,8-nonatetren-1-yl] ether

Suppliers and Price of Retinyl phenyl ether

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 0 raw suppliers

Chemical Property of Retinyl phenyl ether

Chemical Property:

Vapor Pressure:2.12E-09mmHg at 25°C
Boiling Point:493.5°Cat760mmHg
Flash Point:204.1°C
Density:0.977g/cm³
XLogP3:8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:7
Exact Mass:362.260965704
Heavy Atom Count:27
Complexity:619

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CCOC2=CC=CC=C2)C)C
Isomeric SMILES:CC1=C(C(CCC1)(C)C)/C=C/C(=C/C=C/C(=C/COC2=CC=CC=C2)/C)/C

Technology Process of Retinyl phenyl ether

There total 5 articles about Retinyl phenyl ether 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:

: 38987-91-6
5-(2,6,6-trimethyl-cyclohex-1-enyl)-3-methyl-1-phenyl-sulphonyl-penta-2,4-diene

: 75664-68-5
9-Phenoxy-3.7-dimethyl-1t-(2.2.6-trimethyl-cyclohexen-⁽⁶⁾-yl)-nonatetraen-(1.3t.5t.7t)

Guidance literature:: Multi-step reaction with 2 steps

1.1: t-BuOK / dimethylformamide / -20 °C

1.2: 89 percent / dimethylformamide / -20 °C

2.1: 83 percent / NaOEt / ethanol / Heating

With potassium tert-butylate; sodium ethanolate; In ethanol; N,N-dimethyl-formamide; 1.2: Julia sulfone olefination;

Reference yield:

: 114506-04-6
-4-Brom-1-chlor-2-methyl-2-buten

: 75664-68-5
9-Phenoxy-3.7-dimethyl-1t-(2.2.6-trimethyl-cyclohexen-⁽⁶⁾-yl)-nonatetraen-(1.3t.5t.7t)

Guidance literature:: Multi-step reaction with 3 steps

1.1: 97 percent / K₂CO₃ / acetone

2.1: t-BuOK / dimethylformamide / -20 °C

2.2: 89 percent / dimethylformamide / -20 °C

3.1: 83 percent / NaOEt / ethanol / Heating

With potassium tert-butylate; sodium ethanolate; potassium carbonate; In ethanol; N,N-dimethyl-formamide; acetone; 2.2: Julia sulfone olefination;

Reference yield:

: 108-95-2,27073-41-2
phenol

: 75664-68-5
9-Phenoxy-3.7-dimethyl-1t-(2.2.6-trimethyl-cyclohexen-⁽⁶⁾-yl)-nonatetraen-(1.3t.5t.7t)

Guidance literature:: Multi-step reaction with 3 steps

1.1: 97 percent / K₂CO₃ / acetone

2.1: t-BuOK / dimethylformamide / -20 °C

2.2: 89 percent / dimethylformamide / -20 °C

3.1: 83 percent / NaOEt / ethanol / Heating

With potassium tert-butylate; sodium ethanolate; potassium carbonate; In ethanol; N,N-dimethyl-formamide; acetone; 2.2: Julia sulfone olefination;