N-(2-hydroxy-4-nitrophenyl)benzamide

Base Information

Chemical Name:N-(2-hydroxy-4-nitrophenyl)benzamide
CAS No.:38880-89-6
Molecular Formula:C13H10N2O4
Molecular Weight:258.233
Hs Code.:2924299090
European Community (EC) Number:654-027-3
NSC Number:158065
DSSTox Substance ID:DTXSID20392414
Nikkaji Number:J308.246F
Wikidata:Q82190622
ChEMBL ID:CHEMBL245094
Mol file:38880-89-6.mol

Synonyms:N-(2-hydroxy-4-nitrophenyl)benzamide;38880-89-6;2'-Hydroxy-4'-nitrobenzanilide;NSC158065;Oprea1_861233;CHEMBL245094;SCHEMBL11361118;DTXSID20392414;UXCBYNIQABJIOQ-UHFFFAOYSA-N;STK396622;AKOS005431284;N-(2-hydroxy-4-nitro-phenyl)benzamide;NSC-158065;Benzamide, N-(2-hydroxy-4-nitrophenyl)-

Suppliers and Price of N-(2-hydroxy-4-nitrophenyl)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

Sigma-Aldrich
2'-HYDROXY-4'-NITROBENZANILIDE Aldrich
250mg
$ 57.00

American Custom Chemicals Corporation
2'-HYDROXY-4'-NITROBENZANILIDE 95.00%
5MG
$ 498.32

Total 3 raw suppliers

Chemical Property of N-(2-hydroxy-4-nitrophenyl)benzamide

Chemical Property:

Vapor Pressure:1.97E-05mmHg at 25°C
Melting Point:269-270 °C(Solv: ethanol (64-17-5))
Boiling Point:351.8°Cat760mmHg
PKA:8.84±0.19(Predicted)
Flash Point:166.6°C
PSA：95.15000
Density:1.446g/cm³
LogP:3.14890
XLogP3:2.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:258.06405680
Heavy Atom Count:19
Complexity:336

Purity/Quality:: 2'-HYDROXY-4'-NITROBENZANILIDE Aldrich ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)NC2=C(C=C(C=C2)[N+](=O)[O-])O

Technology Process of N-(2-hydroxy-4-nitrophenyl)benzamide

There total 3 articles about N-(2-hydroxy-4-nitrophenyl)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: 92.0%

: 98-88-4
benzoyl chloride

: 121-88-0
5-Nitro-2-aminophenol

: 38880-89-6
N-(2-hydroxy-4-nitrophenyl)benzamide

Guidance literature:: With potassium carbonate; dmap; In tetrahydrofuran; at 23 ℃; for 4h;
DOI:10.1021/ja00222a043

Reference yield: 47.0%

: 3393-96-2
p-nitrobenzanilide

: 38880-89-6
N-(2-hydroxy-4-nitrophenyl)benzamide

Guidance literature:: With dipotassium peroxodisulfate; [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; trifluoroacetic acid; trifluoroacetic anhydride; Reagent/catalyst;
DOI:10.1039/c5sc03905c