(E)-3-(4-methoxy-3-phenylmethoxyphenyl)-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one

Base Information

Chemical Name:(E)-3-(4-methoxy-3-phenylmethoxyphenyl)-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
CAS No.:162442-14-0
Molecular Formula:C₂₆H₂₆O₆
Molecular Weight:434.489
Hs Code.:
European Community (EC) Number:688-605-1

Synonyms:ARKPHARMINC AK279617;162442-14-0;(2E)-3-[3-(benzyloxy)-4-methoxyphenyl]-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one;STL576715;(E)-3-(4-methoxy-3-phenylmethoxyphenyl)-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one

Suppliers and Price of (E)-3-(4-methoxy-3-phenylmethoxyphenyl)-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one

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

Sigma-Aldrich
1-(3-BENZYLOXY-4-METHOXY-PHENYL)-3-(3,4,5-TRIMETHOXY-PHENYL)-PROPENONE Aldrich
1ea
$ 57.00

Total 1 raw suppliers

Chemical Property of (E)-3-(4-methoxy-3-phenylmethoxyphenyl)-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one

Chemical Property:

XLogP3:5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:10
Exact Mass:434.17293854
Heavy Atom Count:32
Complexity:573

Purity/Quality:

98%,99%, ^*data from raw suppliers

1-(3-BENZYLOXY-4-METHOXY-PHENYL)-3-(3,4,5-TRIMETHOXY-PHENYL)-PROPENONE Aldrich ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=C(C=C(C=C1)C=CC(=O)C2=CC(=C(C(=C2)OC)OC)OC)OCC3=CC=CC=C3
Isomeric SMILES:COC1=C(C=C(C=C1)/C=C/C(=O)C2=CC(=C(C(=C2)OC)OC)OC)OCC3=CC=CC=C3

Technology Process of (E)-3-(4-methoxy-3-phenylmethoxyphenyl)-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one

There total 1 articles about (E)-3-(4-methoxy-3-phenylmethoxyphenyl)-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one 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: 92.0%

: 23428-77-5
1‐(3‐(benzyloxy)‐4‐methoxyphenyl)ethanone

: 86-81-7
3,4,5-trimethoxy-benzaldehyde

: 162442-14-0
(E)-1-(3-Benzyloxy-4-methoxy-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propenone

Guidance literature:: With sodium hydroxide; In methanol; at 18 ℃; for 72h;
DOI:10.1039/c39940002647

Reference yield: 96.0%

: 162442-14-0
(E)-1-(3-Benzyloxy-4-methoxy-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propenone

: 162442-15-1
1-(3-hydroxy-4-methoxyphenyl)-3-(3,4,5-trimethoxyphenyl)-1-propanone

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate; at 18 ℃; for 15h; under 760 Torr;
DOI:10.1039/c39940002647

Reference yield:

: 162442-14-0
(E)-1-(3-Benzyloxy-4-methoxy-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propenone

: 143702-43-6
5-[1-Hydroxy-3-(3,4,5-trimethoxy-phenyl)-propyl]-2-methoxy-phenol

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / H₂ / 5percent Pd/C / ethyl acetate / 15 h / 18 °C / 760 Torr

2: 96 percent / NaBH₄ / tetrahydrofuran; methanol / 1.5 h / 18 °C

With sodium tetrahydroborate; hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; ethyl acetate;
DOI:10.1039/c39940002647