4H-1-Benzopyran-4-one, 7-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-

Base Information

Chemical Name:4H-1-Benzopyran-4-one, 7-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-
CAS No.:29376-69-0
Molecular Formula:C₂₀H₁₆O₇
Molecular Weight:368.343
Hs Code.:
DSSTox Substance ID:DTXSID801155943
Nikkaji Number:J127.324H
Mol file:29376-69-0.mol

Synonyms:29376-69-0;7-Acetoxy-2-(4-acetoxyphenyl)-5-methoxy-4H-1-benzopyran-4-one;4H-1-Benzopyran-4-one, 7-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-;DTXSID801155943;4-[7-(Acetyloxy)-5-methoxy-4-oxo-4H-chromen-2-yl]phenyl acetate #;7-(Acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-4H-1-benzopyran-4-one

Suppliers and Price of 4H-1-Benzopyran-4-one, 7-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-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 3 raw suppliers

Chemical Property of 4H-1-Benzopyran-4-one, 7-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-

Chemical Property:

PSA：92.04000
LogP:3.31920
XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:6
Exact Mass:368.08960285
Heavy Atom Count:27
Complexity:618

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC(=O)C

Technology Process of 4H-1-Benzopyran-4-one, 7-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-

There total 4 articles about 4H-1-Benzopyran-4-one, 7-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-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:

: 480-41-1
5,7-Dihydroxy-2-(4-hydroxy-phenyl)-chroman-4-on

: 29376-69-0
Thevetiaflavon-diacetat

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine

2: potassium carbonate

3: acetic acid anhydride; selenium dioxide

With pyridine; selenium(IV) oxide; acetic anhydride; potassium carbonate;

Reference yield:

: 108977-51-1
naringenin 5-methyl ether 7,4'-diacetate

: 29376-69-0
Thevetiaflavon-diacetat

Guidance literature:: With selenium(IV) oxide; acetic anhydride;

Reference yield:

: 3162-03-6
2-(4-acetoxyphenyl)-5-hydroxy-4-oxochroman-7-yl acetate

: 29376-69-0
Thevetiaflavon-diacetat

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate

2: acetic acid anhydride; selenium dioxide

With selenium(IV) oxide; acetic anhydride; potassium carbonate;