1-(4-Isopropoxy-3-methoxyphenyl)-3-(4-isopropoxy-3-methoxybenzyl)-5,7-diisopropoxy-2-methylnaphthalene

Base Information

Chemical Name:1-(4-Isopropoxy-3-methoxyphenyl)-3-(4-isopropoxy-3-methoxybenzyl)-5,7-diisopropoxy-2-methylnaphthalene
CAS No.:133773-24-7
Molecular Formula:C₃₈H₄₈O₆
Molecular Weight:600.796
Hs Code.:

Synonyms:1-(4-Isopropoxy-3-methoxyphenyl)-3-(4-isopropoxy-3-methoxybenzyl)-5,7-diisopropoxy-2-methylnaphthalene

Suppliers and Price of 1-(4-Isopropoxy-3-methoxyphenyl)-3-(4-isopropoxy-3-methoxybenzyl)-5,7-diisopropoxy-2-methylnaphthalene

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 1-(4-Isopropoxy-3-methoxyphenyl)-3-(4-isopropoxy-3-methoxybenzyl)-5,7-diisopropoxy-2-methylnaphthalene

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-(4-Isopropoxy-3-methoxyphenyl)-3-(4-isopropoxy-3-methoxybenzyl)-5,7-diisopropoxy-2-methylnaphthalene

There total 24 articles about 1-(4-Isopropoxy-3-methoxyphenyl)-3-(4-isopropoxy-3-methoxybenzyl)-5,7-diisopropoxy-2-methylnaphthalene 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: 80.0%

: 133593-79-0
[3-Hydroxymethyl-6,8-diisopropoxy-4-(4-isopropoxy-3-methoxy-phenyl)-naphthalen-2-yl]-(4-isopropoxy-3-methoxy-phenyl)-methanol

: 133773-24-7
1-(4-Isopropoxy-3-methoxyphenyl)-3-(4-isopropoxy-3-methoxybenzyl)-5,7-diisopropoxy-2-methylnaphthalene

Guidance literature:: With hydrogen; triethylamine; trifluoroacetic anhydride; palladium on activated charcoal; In tetrahydrofuran; for 18h;
DOI:10.1039/c39910000190

Reference yield:

: 88275-87-0
3-bromo-2-methyloxybenzaldehyde

: 133773-24-7
1-(4-Isopropoxy-3-methoxyphenyl)-3-(4-isopropoxy-3-methoxybenzyl)-5,7-diisopropoxy-2-methylnaphthalene

Guidance literature:: Multi-step reaction with 13 steps

1: 91 percent / benzene / 20 h / Heating

2: 95 percent / 90percent aq. TFA / 0.25 h

3: 84 percent / KOAc / 0.08 h / Heating

4: 94 percent / diisobutylaluminium hydride / hexane; tetrahydrofuran / 0.17 h

5: 82 percent / K₂CO₃ / toluene / 96 h

7: 95 percent / toluene / 12 h / Heating

8: 85 percent / aq. NaOH / methanol / 96 h / Heating

10: 88 percent / tetrahydrofuran / 0.5 h / Ambient temperature

12: 99 percent / LiAlH₄ / diethyl ether / 2 h / Ambient temperature

13: 80 percent / H₂, NEt₃, trifluoroacetic anhydride / 10percent Pd/C / tetrahydrofuran / 18 h

With sodium hydroxide; lithium aluminium tetrahydride; hydrogen; potassium acetate; diisobutylaluminium hydride; potassium carbonate; triethylamine; trifluoroacetic acid; trifluoroacetic anhydride; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; hexane; toluene; benzene;

Reference yield:

: 133593-75-6
4,5-Dihydro-2-(5,7-diisopropoxy-1-methoxy-2-naphthyl)-4,4-dimethyloxazole

: 133773-24-7
1-(4-Isopropoxy-3-methoxyphenyl)-3-(4-isopropoxy-3-methoxybenzyl)-5,7-diisopropoxy-2-methylnaphthalene

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / tetrahydrofuran / 0.5 h / Ambient temperature

3: 99 percent / LiAlH₄ / diethyl ether / 2 h / Ambient temperature

4: 80 percent / H₂, NEt₃, trifluoroacetic anhydride / 10percent Pd/C / tetrahydrofuran / 18 h

With lithium aluminium tetrahydride; hydrogen; triethylamine; trifluoroacetic anhydride; palladium on activated charcoal; In tetrahydrofuran; diethyl ether;