Benzamide, 4-hydroxy-N-(2-hydroxyphenyl)-

Base Information

Chemical Name:Benzamide, 4-hydroxy-N-(2-hydroxyphenyl)-
CAS No.:174412-29-4
Molecular Formula:C13H11NO3
Molecular Weight:229.235
Hs Code.:
ChEMBL ID:CHEMBL117760
DSSTox Substance ID:DTXSID80466549
Wikidata:Q82293137

Synonyms:Benzamide, 4-hydroxy-N-(2-hydroxyphenyl)-;174412-29-4;CHEMBL117760;SCHEMBL3661213;DTXSID80466549

Suppliers and Price of Benzamide, 4-hydroxy-N-(2-hydroxyphenyl)-

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 1 raw suppliers

Chemical Property of Benzamide, 4-hydroxy-N-(2-hydroxyphenyl)-

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:229.07389321
Heavy Atom Count:17
Complexity:261

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C(=C1)NC(=O)C2=CC=C(C=C2)O)O

Technology Process of Benzamide, 4-hydroxy-N-(2-hydroxyphenyl)-

There total 3 articles about Benzamide, 4-hydroxy-N-(2-hydroxyphenyl)- 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: 62.0%

: 7464-55-3
N-(o-methoxyphenyl)-4-methoxybenzamide

: 174412-29-4
4-hydroxy-N-(2-hydroxyphenyl)benzamide

Guidance literature:: With boron tribromide; In dichloromethane; at 0 - 20 ℃; for 0.5h;
DOI:10.1016/j.ejmech.2017.03.086

Reference yield:

: 90-04-0
2-methoxy-phenylamine

: 174412-29-4
4-hydroxy-N-(2-hydroxyphenyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: 1,1'-carbonyldiimidazole / acetonitrile / 0.5 h / 20 °C / Inert atmosphere

1.2: 20 °C / Inert atmosphere

2.1: boron tribromide / dichloromethane / 0.5 h / 0 - 20 °C

With boron tribromide; 1,1'-carbonyldiimidazole; In dichloromethane; acetonitrile;
DOI:10.1016/j.ejmech.2017.03.086

Reference yield:

: 100-09-4
4-methoxybenzoic acid

: 174412-29-4
4-hydroxy-N-(2-hydroxyphenyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: 1,1'-carbonyldiimidazole / acetonitrile / 0.5 h / 20 °C / Inert atmosphere

1.2: 20 °C / Inert atmosphere

2.1: boron tribromide / dichloromethane / 0.5 h / 0 - 20 °C

With boron tribromide; 1,1'-carbonyldiimidazole; In dichloromethane; acetonitrile;
DOI:10.1016/j.ejmech.2017.03.086