2,4-Dihydroxy-N-(2-hydroxyethyl)benzamide

Base Information

• Chemical Name: 2,4-Dihydroxy-N-(2-hydroxyethyl)benzamide
• CAS No.: 24207-41-8
• Molecular Formula: C9H11NO4
• Molecular Weight: 197.191
• Hs Code.: 2924299090
• European Community (EC) Number: 246-077-6
• NSC Number: 379528
• UNII: ERN2T4Z42W
• DSSTox Substance ID: DTXSID9066968
• Nikkaji Number: J141.523I
• Wikidata: Q72466671
• Mol file: 24207-41-8.mol

Synonyms:2,4-Dihydroxy-N-(2-hydroxyethyl)benzamide;24207-41-8;Benzamide, 2,4-dihydroxy-N-(2-hydroxyethyl)-;ERN2T4Z42W;EINECS 246-077-6;NSC 379528;NSC-379528;NSC379528;UNII-ERN2T4Z42W;SCHEMBL4913264;DTXSID9066968;beta-Resorcylic acid ethanolamide;AKOS009129733;N-(2-Hydroxyethyl)-.beta.-resorcylamide;.beta.-Resorcylamide, N-(2-hydroxyethyl)-;CS-0229977;FT-0638404;EN300-101801;2,4-Dihydroxy-N-(2-hydroxyethyl)benzamide, 96%

Chemical Property of 2,4-Dihydroxy-N-(2-hydroxyethyl)benzamide

Chemical Property:

• Appearance/Colour: beige crystalline powder
• Melting Point: 163-165 ºC
• Boiling Point: 547.1 °C at 760 mmHg
• PKA: 8.08±0.35(Predicted)
• Flash Point: 284.7 °C
• PSA: 89.79000
• Density: 1.401 g/cm³
• LogP: 0.21080
• XLogP3: 0.7
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 197.06880783
• Heavy Atom Count: 14
• Complexity: 197

Purity/Quality:

99.0%Min ^*data from raw suppliers

2,4-Dihydroxy-N-(2-hydroxyethyl)benzamide 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39

MSDS Files:

Useful:

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

Technology Process of 2,4-Dihydroxy-N-(2-hydroxyethyl)benzamide

There total 2 articles about 2,4-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:

methyl 2,4-dihydroxybenzoate (2150-47-2) → 2,4-dihydroxy-N-(2-hydroxy-ethyl)benzamide (24207-41-8)

Guidance literature:

Reference yield:

→ 2,4-dihydroxy-N-(2-hydroxy-ethyl)benzamide (24207-41-8)

Guidance literature:

Entspr. Carbonsaeure, H2NCH2CH2OH;

Reference yield:

2,4-dihydroxy-N-(2-hydroxy-ethyl)benzamide (24207-41-8) + 2-benzyl-3-chloro-3-phenyl-2,3-dihydroisoindol-1-one (237769-24-3) → N-[2-(2-benzyl-3-oxo-1-phenyl-2,3-dihydro-1H-isoindol-1-yloxy)ethyl]-2,4-dihydroxybenzamide

Guidance literature:

In tetrahydrofuran; at 20 ℃; for 72h;

DOI:10.1021/jm0601194

upstream raw materials:

methyl 2,4-dihydroxybenzoate