N-(3-oxo-1,3-dihydro-2-benzofuran-5-yl)acetamide

Base Information

Chemical Name:N-(3-oxo-1,3-dihydro-2-benzofuran-5-yl)acetamide
CAS No.:21626-90-4
Molecular Formula:C10H9NO3
Molecular Weight:191.186
Hs Code.:
DSSTox Substance ID:DTXSID40358517
Wikidata:Q82139141
Mol file:21626-90-4.mol

Synonyms:21626-90-4;N-(3-oxo-1,3-dihydro-2-benzofuran-5-yl)acetamide;SCHEMBL2195036;DTXSID40358517;N-(3-Oxo-1,3-dihydroisobenzofuran-5-yl)acetamide

Suppliers and Price of N-(3-oxo-1,3-dihydro-2-benzofuran-5-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
Packaging
price

Total 0 raw suppliers

Chemical Property of N-(3-oxo-1,3-dihydro-2-benzofuran-5-yl)acetamide

Chemical Property:

XLogP3:0
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:191.058243149
Heavy Atom Count:14
Complexity:264

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=CC2=C(COC2=O)C=C1

Technology Process of N-(3-oxo-1,3-dihydro-2-benzofuran-5-yl)acetamide

There total 1 articles about N-(3-oxo-1,3-dihydro-2-benzofuran-5-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:

: 5-amino-2-hydroxymethyl-benzoic acid hydrazide

: 108-24-7
acetic anhydride

: 21626-90-4
6-acetylaminophthalide

: 1068-57-1
acetic acid hydrazide

Guidance literature:: beim Kochen;

Reference yield:

: 21626-90-4
6-acetylaminophthalide

: 146850-12-6
2-methyl-1H-furo<3,4-e>benzimidazol-8(6H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / sulfuric acid, potassium nitrate / 1 h / Ambient temperature

2: 76 percent / stannous chloride / ethyl acetate / 1 h / Heating

With sulfuric acid; potassium nitrate; tin(ll) chloride; In ethyl acetate;