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o-Oxalotoluidide

Base Information Edit
  • Chemical Name:o-Oxalotoluidide
  • CAS No.:3299-62-5
  • Molecular Formula:C16H16N2O2
  • Molecular Weight:268.315
  • Hs Code.:2924299090
  • European Community (EC) Number:665-999-3
  • NSC Number:11023
  • DSSTox Substance ID:DTXSID60279013
  • Wikidata:Q82011271
  • ChEMBL ID:CHEMBL1504147
  • Mol file:3299-62-5.mol
o-Oxalotoluidide

Synonyms:o-Oxalotoluidide;3299-62-5;N1,N2-Di-o-tolyloxalamide;N,N'-bis(2-methylphenyl)oxamide;MLS000737936;CHEMBL1504147;N,N'-bis(2-methylphenyl)ethanediamide;o-Oxotoluidide;Ditolyloxamid;NSC11023;NSC 11023;N,N'-bis(o-tolyl)oxamide;SCHEMBL2344209;DTXSID60279013;N,N'-DI(O-TOLYL)OXAMIDE;HMS2886P15;BDBM50350694;NSC-11023;STK061965;AKOS000340095;SMR000528095;FT-0673323

Suppliers and Price of o-Oxalotoluidide
Supply Marketing:Edit
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
  • TRC
  • o-Oxalotoluidide
  • 10g
  • $ 1100.00
  • Sigma-Aldrich
  • N,N'-DI(O-TOLYL)OXAMIDE Aldrich
  • 1ea
  • $ 144.00
  • American Custom Chemicals Corporation
  • N,N'-DI(O-TOLYL)OXAMIDE 95.00%
  • 5MG
  • $ 503.11
Total 7 raw suppliers
Chemical Property of o-Oxalotoluidide Edit
Chemical Property:
  • Melting Point:215 °C 
  • PKA:11.11±0.70(Predicted) 
  • PSA:58.20000 
  • Density:1.241±0.06 g/cm3(Predicted) 
  • LogP:3.02660 
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:268.121177757
  • Heavy Atom Count:20
  • Complexity:322
Purity/Quality:

o-Oxalotoluidide *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC=CC=C1NC(=O)C(=O)NC2=CC=CC=C2C
Technology Process of o-Oxalotoluidide

There total 18 articles about o-Oxalotoluidide 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 triethylamine; In 1,4-dioxane; at 0 ℃;
DOI:10.1016/S0040-4020(01)00360-X
Guidance literature:
With sodium; In ethanol; for 1h; Heating;
DOI:10.3390/50500714
Guidance literature:
With 4 A molecular sieve; In toluene; acetonitrile; at 150 ℃; 2 d; 2 d;
DOI:10.1016/0040-4020(95)00735-Q
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