3,5-Dihydroxy-N-(2-hydroxyethyl)benzamide

Base Information

Chemical Name:3,5-Dihydroxy-N-(2-hydroxyethyl)benzamide
CAS No.:21734-43-0
Molecular Formula:C9H11 N O4
Molecular Weight:197.191
Hs Code.:2924299090
European Community (EC) Number:244-552-2
DSSTox Substance ID:DTXSID7066728
Nikkaji Number:J181.445A
Wikidata:Q81993310
Mol file:21734-43-0.mol

Synonyms:3,5-Dihydroxy-N-(2-hydroxyethyl)benzamide;21734-43-0;Benzamide, 3,5-dihydroxy-N-(2-hydroxyethyl)-;3,5-Resorcylic acid ethanolamide;Oprea1_517493;SCHEMBL5878629;DTXSID7066728;EINECS 244-552-2;MFCD00129719;STK164608;AKOS003268408;LS-08393;N-(2-Hydroxyethyl)-3,5-dihydroxybenzamide;CS-0315045

Suppliers and Price of 3,5-Dihydroxy-N-(2-hydroxyethyl)benzamide

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

Matrix Scientific
3,5-Dihydroxy-N-(2-hydroxyethyl)benzamide
1g
$ 200.00

Matrix Scientific
3,5-Dihydroxy-N-(2-hydroxyethyl)benzamide
0.500g
$ 160.00

Matrix Scientific
3,5-Dihydroxy-N-(2-hydroxyethyl)benzamide
5g
$ 700.00

Crysdot
3,5-Dihydroxy-N-(2-hydroxyethyl)benzamide 97%
5g
$ 527.00

Total 7 raw suppliers

Chemical Property of 3,5-Dihydroxy-N-(2-hydroxyethyl)benzamide

Chemical Property:

Vapor Pressure:1.12E-12mmHg at 25°C
Boiling Point:544.2°Cat760mmHg
Flash Point:282.9°C
PSA：93.28000
Density:1.401g/cm³
LogP:0.39470
XLogP3:0.3
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:197.06880783
Heavy Atom Count:14
Complexity:187

Purity/Quality:

99% ^*data from raw suppliers

3,5-Dihydroxy-N-(2-hydroxyethyl)benzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=C(C=C(C=C1O)O)C(=O)NCCO

Technology Process of 3,5-Dihydroxy-N-(2-hydroxyethyl)benzamide

There total 5 articles about 3,5-Dihydroxy-N-(2-hydroxyethyl)benzamide 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:

: C₂₃H₂₃NO₄

: 21734-43-0
N-(2-hydroxyethyl)-3,5-dihydroxybenzamide

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In ethanol; ethyl acetate; at 20 ℃; for 16h; under 760.051 Torr;
DOI:10.1039/c9ob01459d

Reference yield:

: 99-10-5
3,5-Dihydroxybenzoic acid

: 21734-43-0
N-(2-hydroxyethyl)-3,5-dihydroxybenzamide

Guidance literature:: Multi-step reaction with 5 steps

1: sulfuric acid / methanol / 5 h / Inert atmosphere; Reflux

2: potassium carbonate / 20 °C / Inert atmosphere

3: potassium hydroxide / ethanol / 2 h / Inert atmosphere; Reflux

4: 24 h / 0 - 20 °C / Inert atmosphere; Alkaline conditions

5: palladium 10% on activated carbon; hydrogen / ethanol; ethyl acetate / 16 h / 20 °C / 760.05 Torr

With sulfuric acid; palladium 10% on activated carbon; hydrogen; potassium carbonate; potassium hydroxide; In methanol; ethanol; ethyl acetate;
DOI:10.1039/c9ob01459d

Reference yield:

: 2150-44-9
1-carbomethoxy-3,5-dihydroxybenzene

: 21734-43-0
N-(2-hydroxyethyl)-3,5-dihydroxybenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / 20 °C / Inert atmosphere

2: potassium hydroxide / ethanol / 2 h / Inert atmosphere; Reflux

3: 24 h / 0 - 20 °C / Inert atmosphere; Alkaline conditions

4: palladium 10% on activated carbon; hydrogen / ethanol; ethyl acetate / 16 h / 20 °C / 760.05 Torr

With palladium 10% on activated carbon; hydrogen; potassium carbonate; potassium hydroxide; In ethanol; ethyl acetate;
DOI:10.1039/c9ob01459d