Benzamide, 5-(acetylamino)-2-hydroxy-

Base Information

Chemical Name:Benzamide, 5-(acetylamino)-2-hydroxy-
CAS No.:13913-32-1
Molecular Formula:C₉H₁₀N₂O₃
Molecular Weight:194.19
Hs Code.:
DSSTox Substance ID:DTXSID80438180
Nikkaji Number:J623.679K
Wikidata:Q82253828
ChEMBL ID:CHEMBL3629434

Synonyms:5-acetamido-2-hydroxybenzamide;13913-32-1;Benzamide, 5-(acetylamino)-2-hydroxy-;5-acetamidosalicylamide;SCHEMBL551783;CHEMBL3629434;DTXSID80438180;YXRPUZIIKDKSNR-UHFFFAOYSA-N;2-Hydroxy-5-(acetylamino)benzamide

Suppliers and Price of Benzamide, 5-(acetylamino)-2-hydroxy-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of Benzamide, 5-(acetylamino)-2-hydroxy-

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:194.06914219
Heavy Atom Count:14
Complexity:242

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=CC(=C(C=C1)O)C(=O)N

Technology Process of Benzamide, 5-(acetylamino)-2-hydroxy-

There total 4 articles about Benzamide, 5-(acetylamino)-2-hydroxy- 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:

: 122228-38-0
Methyl 5-acetylamino-2-acetyloxybenzoate

: 13913-32-1
5-Acetylamino-2-hydroxybenzamide

Guidance literature:: With ammonium hydroxide; at 20 ℃;
DOI:10.3109/00498259509061869

Reference yield:

: 89-57-6
5-Aminosalicylic Acid

: 13913-32-1
5-Acetylamino-2-hydroxybenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂ / 48 h / 20 °C

2: H₂SO₄ / CHCl₃

3: 2.0 g / 28 percent aq. NH₃ / 20 °C

With ammonium hydroxide; thionyl chloride; sulfuric acid; In chloroform; 1: Esterification / 2: Acetylation / 3: Substitution;
DOI:10.3109/00498259509061869

Reference yield:

: 42753-75-3
methyl 5-amino-2-hydroxybenzoate

: 13913-32-1
5-Acetylamino-2-hydroxybenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: H₂SO₄ / CHCl₃

2: 2.0 g / 28 percent aq. NH₃ / 20 °C

With ammonium hydroxide; sulfuric acid; In chloroform; 1: Acetylation / 2: Substitution;
DOI:10.3109/00498259509061869