N-(4-oxo-2-phenylchromen-6-yl)acetamide

Base Information

Chemical Name:N-(4-oxo-2-phenylchromen-6-yl)acetamide
CAS No.:18467-10-2
Molecular Formula:C17H13NO3
Molecular Weight:279.295
Hs Code.:
DSSTox Substance ID:DTXSID90393534
Wikidata:Q82192334
ChEMBL ID:CHEMBL1215385

Synonyms:18467-10-2;N-(4-Oxo-2-phenyl-4H-chromen-6-yl)acetamide;N-(4-oxo-2-phenylchromen-6-yl)acetamide;6-acetamidoflavone;N-(4-oxo-2-phenyl-chromen-6-yl)acetamide;Oprea1_169799;CHEMBL1215385;SCHEMBL17786530;DTXSID90393534

Suppliers and Price of N-(4-oxo-2-phenylchromen-6-yl)acetamide

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
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price

Total 1 raw suppliers

Chemical Property of N-(4-oxo-2-phenylchromen-6-yl)acetamide

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:279.08954328
Heavy Atom Count:21
Complexity:451

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=CC2=C(C=C1)OC(=CC2=O)C3=CC=CC=C3

Technology Process of N-(4-oxo-2-phenylchromen-6-yl)acetamide

There total 11 articles about N-(4-oxo-2-phenylchromen-6-yl)acetamide 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: 96.0%

: 52923-34-9
N-[4-hydroxy-3-[(E)-3-phenylprop-2-enoyl]phenyl]acetamide

: 18467-10-2
N-(4-oxo-2-phenyl-4H-chromen-6-yl)acetamide

Guidance literature:: With iodine; In dimethyl sulfoxide; at 140 ℃; for 0.366667h; Microwave irradiation;

Reference yield: 85.0%

: 24449-58-9
5′-acetamino-2′-hydroxychalcone

: 18467-10-2
N-(4-oxo-2-phenyl-4H-chromen-6-yl)acetamide

Guidance literature:: With iodine; In dimethyl sulfoxide; for 0.5h; Heating;

Reference yield:

: 7298-67-1
5-acetamido-2-hydroxyacetophenone

: 18467-10-2
N-(4-oxo-2-phenyl-4H-chromen-6-yl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium

2: acetic acid; concentrated aqueous hydrochloric acid / 120 °C

With hydrogenchloride; sodium; acetic acid;
DOI:10.1021/jo01099a604