4-Flavanol, 4'-methoxy-

Base Information

Chemical Name:4-Flavanol, 4'-methoxy-
CAS No.:5162-64-1
Molecular Formula:C16H16O3
Molecular Weight:256.301
Hs Code.:2932999099
DSSTox Substance ID:DTXSID501217671
Nikkaji Number:J144.325I
Mol file:5162-64-1.mol

Synonyms:4-Flavanol, 4'-methoxy-;5162-64-1;3,4-Dihydro-2-(4-methoxyphenyl)-2H-1-benzopyran-4-ol;2H-1-Benzopyran-4-ol, 3,4-dihydro-2-(4-methoxyphenyl)-;4'-Methoxy-4-flavanol;DTXSID501217671;2-(4-Methoxyphenyl)-4-chromanol #

Suppliers and Price of 4-Flavanol, 4'-methoxy-

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 4 raw suppliers

Chemical Property of 4-Flavanol, 4'-methoxy-

Chemical Property:

PSA：38.69000
LogP:3.25240
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:256.109944368
Heavy Atom Count:19
Complexity:286

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)C2CC(C3=CC=CC=C3O2)O

Technology Process of 4-Flavanol, 4'-methoxy-

There total 42 articles about 4-Flavanol, 4'-methoxy- 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: 94.0%

: 3034-08-0,93921-53-0,97005-76-0
2-(4-methoxyphenyl)-2,3-dihydro-4H-chromen-4-one

: 5162-64-1,34811-92-2,40106-97-6,55568-94-0,62137-47-7,88269-27-6
(+/-)-cis-4'-methoxyflavan-4-ol

Guidance literature:: With sodium tetrahydroborate; at 20 ℃; for 1h; enantioselective reaction; Cooling with ice;
DOI:10.1016/j.mcat.2021.111734

Reference yield: 90.0%

: 34000-29-8
[E]-3-(p-methoxyphenyl)-1-(2-hydroxyphenyl)prop-2-en-1-one

: 5162-64-1,34811-92-2,40106-97-6,55568-94-0,62137-47-7,88269-27-6
(+/-)-cis-4'-methoxyflavan-4-ol

Guidance literature:: With sodium hydroxide; sodium tetrahydroborate; tetra(n-butyl)ammonium hydrogensulfate; In dichloromethane; Ambient temperature;