3-((2-Hydroxyethyl)carbamoyl)-5-nitrobenzoic acid

Base Information

• Chemical Name: 3-((2-Hydroxyethyl)carbamoyl)-5-nitrobenzoic acid
• CAS No.: 22871-56-3
• Molecular Formula: C10H10 N2 O6
• Molecular Weight: 254.199
• Hs Code.: 2924299090
• European Community (EC) Number: 245-274-4
• UNII: 8KN7288AQ4
• DSSTox Substance ID: DTXSID70177410
• Nikkaji Number: J286.330H
• Wikidata: Q72484021
• Mol file: 22871-56-3.mol

Synonyms:22871-56-3;3-((2-Hydroxyethyl)carbamoyl)-5-nitrobenzoic acid;3-(2-hydroxyethylcarbamoyl)-5-nitrobenzoic acid;3-[[(2-HYDROXYETHYL)AMINO]CARBONYL]-5-NITROBENZOIC ACID;3-(((2-Hydroxyethyl)amino)carbonyl)-5-nitrobenzoic acid;EINECS 245-274-4;8KN7288AQ4;Benzoic acid, 3-(((2-hydroxyethyl)amino)carbonyl)-5-nitro-;3-((2-Hydroxyethyl)carbamoyl)-5-nitrobenzoicacid;UNII-8KN7288AQ4;DTXSID70177410;AKOS015999499;A878409;W-110552

Chemical Property of 3-((2-Hydroxyethyl)carbamoyl)-5-nitrobenzoic acid

Chemical Property:

• Vapor Pressure: 2.08E-11mmHg at 25°C
• Melting Point: 186 °C
• Refractive Index: 1.625
• Boiling Point: 514.5°Cat760mmHg
• PKA: 3.20±0.10(Predicted)
• Flash Point: 264.9°C
• PSA: 132.45000
• Density: 1.511g/cm³
• LogP: 0.92920
• Storage Temp.: 2-8°C
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4
• Exact Mass: 254.05388604
• Heavy Atom Count: 18
• Complexity: 340

Purity/Quality:

99% ^*data from raw suppliers

3-((2-Hydroxyethyl)carbamoyl)-5-nitrobenzoicacid 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(C=C(C=C1C(=O)O)[N+](=O)[O-])C(=O)NCCO

Technology Process of 3-((2-Hydroxyethyl)carbamoyl)-5-nitrobenzoic acid

There total 1 articles about 3-((2-Hydroxyethyl)carbamoyl)-5-nitrobenzoic acid 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:

→ 3-{[(2-hydroxyethyl)amino]carbonyl}-5-nitrobenzoic acid (22871-56-3)

Guidance literature:

/BRN= 886334/, Ethanolamin;