2-(4-(DiMethylaMino)phenyl)-7,8-diMethoxy-4H-chroMen-4-one HBr

Base Information

Chemical Name:2-(4-(DiMethylaMino)phenyl)-7,8-diMethoxy-4H-chroMen-4-one HBr
CAS No.:1205548-03-3
Molecular Formula:C19H20BrNO4
Molecular Weight:325.364
Hs Code.:2922509090
Mol file:1205548-03-3.mol

Synonyms:2-(4-(DiMethylaMino)phenyl)-7,8-diMethoxy-4H-chroMen-4-one HBr;2-(4-(Dimethylamino)phenyl)-7,8-dimethoxy-4H-chromen-4-one hydrobromide;4'-DiMethylaMino 7,8-Dihydroxyflavone DiMethyl Ether

Suppliers and Price of 2-(4-(DiMethylaMino)phenyl)-7,8-diMethoxy-4H-chroMen-4-one HBr

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

TRC
4''-Dimethylamino7,8-DihydroxyflavoneDimethylEther
250mg
$ 1210.00

TRC
4''-Dimethylamino7,8-DihydroxyflavoneDimethylEther
25mg
$ 155.00

Medical Isotopes, Inc.
4??-Dimethylamino7,8-DihydroxyflavoneDimethylEther
250 mg
$ 2000.00

Total 3 raw suppliers

Chemical Property of 2-(4-(DiMethylaMino)phenyl)-7,8-diMethoxy-4H-chroMen-4-one HBr

Chemical Property:

PSA：51.91000
LogP:4.50130
Storage Temp.:Refrigerator
Solubility.:Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly, Heated)

Purity/Quality:

98%min ^*data from raw suppliers

4''-Dimethylamino7,8-DihydroxyflavoneDimethylEther ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 4''-Dimethylamino 7,8-Dihydroxyflavone Dimethyl Ether is a 7,8-Dihydroxyflavone (D452830) derivative which promotes neurogenesis and exhibits potent antidepressant effect. 4'-Dimethylamino 7,8-Dihydroxyflavone Dimethyl Ether is a 7,8-Dihydroxyflavone (D452830) derivative which promotes neurogenesis and exhibits potent antidepressant effect.

Technology Process of 2-(4-(DiMethylaMino)phenyl)-7,8-diMethoxy-4H-chroMen-4-one HBr

There total 5 articles about 2-(4-(DiMethylaMino)phenyl)-7,8-diMethoxy-4H-chroMen-4-one HBr 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: 78.0%

: (E)-3-(4-(dimethylamino)phenyl)-1-(2-hydroxy-3,4-dimethoxyphenyl)prop-2-en-1-one

: 1205548-03-3
2-(4-(dimethylamino)phenyl)-7,8-dimethoxy-4H-chromen-4-one

Guidance literature:: With iodine; In dimethyl sulfoxide; at 130 ℃; for 5 - 6h;
DOI:10.1016/j.bmc.2013.10.012

Reference yield: 44.0%

: 1205548-02-2
1-(4-(dimethylamino)phenyl)-3-(2-hydroxy-3,4-dimethoxyphenyl)propane-1,3-dione

: 1205548-03-3
2-(4-(dimethylamino)phenyl)-7,8-dimethoxy-4H-chromen-4-one

Guidance literature:: With sulfuric acid; acetic acid; for 1 - 3h; Reflux;
DOI:10.1016/j.bmc.2013.10.012

Reference yield:

: 4755-50-4
4-(dimethylamino)benzoyl chloride

: 1205548-03-3
2-(4-(dimethylamino)phenyl)-7,8-dimethoxy-4H-chromen-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / dichloromethane / 20 °C

2: pyridine; potassium hydroxide / 12 h / 50 °C

3: acetic acid; sulfuric acid / 1 - 3 h / Reflux

With pyridine; sulfuric acid; acetic acid; potassium hydroxide; In dichloromethane; 2: |Baker-Venkataraman Rearrangement;
DOI:10.1016/j.bmc.2013.10.012