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2-nitro-N-(2-phenylethyl)benzamide

Base Information
  • Chemical Name:2-nitro-N-(2-phenylethyl)benzamide
  • CAS No.:19209-03-1
  • Molecular Formula:C15H14N2O3
  • Molecular Weight:270.288
  • Hs Code.:
  • DSSTox Substance ID:DTXSID301328230
  • ChEMBL ID:CHEMBL1500180
2-nitro-N-(2-phenylethyl)benzamide

Synonyms:2-nitro-N-(2-phenylethyl)benzamide;2-Nitro-N-phenethyl-benzamide;Oprea1_027826;Oprea1_134962;19209-03-1;MLS001212534;CHEMBL1500180;DTXSID301328230;HMS2835I05;STL362921;AKOS000541211;SMR000515936

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2-nitro-N-(2-phenylethyl)benzamide
Chemical Property:
  • XLogP3:2.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:270.10044231
  • Heavy Atom Count:20
  • Complexity:335
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C(C=C1)CCNC(=O)C2=CC=CC=C2[N+](=O)[O-]
Technology Process of 2-nitro-N-(2-phenylethyl)benzamide

There total 6 articles about 2-nitro-N-(2-phenylethyl)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:
Guidance literature:
With dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; N,N-dimethyl-formamide; at 60 ℃; for 4h;
DOI:10.1021/acs.orglett.0c02032
Guidance literature:
With pyridine; In benzene; at 20 ℃;
DOI:10.1002/jccs.200500135
Guidance literature:
With tert.-butylhydroperoxide; 1-(3-sulfopropyl)pyridinium phosphotungstate; In water; at 90 ℃; for 1h; Microwave irradiation; Green chemistry;
DOI:10.1016/j.tet.2016.11.002
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