p-Oxalotoluidide

Base Information Edit

Chemical Name:p-Oxalotoluidide
CAS No.:3299-61-4
Molecular Formula:C16H16N2O2
Molecular Weight:268.315
Hs Code.:2924299090
NSC Number:401961
UNII:VXW61IZ0NZ
DSSTox Substance ID:DTXSID10186622
Nikkaji Number:J42.593A
Wikidata:Q83057969
Mol file:3299-61-4.mol

Synonyms:p-Oxalotoluidide;3299-61-4;N,N'-bis(4-methylphenyl)oxamide;N,N'-Di-p-tolyloxamide;NSC 401961;Ethanediamide, N,N'-bis(4-methylphenyl)-;OXAMIDE, N,N'-DI-p-TOLYL-;VXW61IZ0NZ;BRN 2136359;N,N'-Bis(4-tolyl)oxamide;NSC-401961;3-12-00-02072 (Beilstein Handbook Reference);Ethanediamide, N,N'-bis(4-methylphenyl)- (9CI);NSC401961;di-(p-tolyl)oxamide;N1,N2-Bis(4-methylphenyl)ethanediamide;UNII-VXW61IZ0NZ;Oxamide,N'-di-p-tolyl-;N,N'-bis(p-tolyl)oxamide;N1,N2-Di-p-tolyloxalamide;N,N'-bis(p-tolyl)-oxamide;SCHEMBL6850999;DTXSID10186622;N-(4-Methylphenyl)-N'-(4-methylphenyl)ethane-1,2-diamide;N,N/'-Bis(4-methylphenyl)oxamide;STK150974;AKOS001023218;N,N'-bis(4-methylphenyl)ethanediamide;Ethanediamide,N'-bis(4-methylphenyl)-;LS-99531;CS-0362446;FT-0673324;ETHANEDIAMIDE, N1,N2-BIS(4-METHYLPHENYL)-;Z56755346

Suppliers and Price of p-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

Usbiological
p-Oxalotoluidide
500mg
$ 432.00

TRC
p-Oxalotoluidide
10g
$ 1100.00

American Custom Chemicals Corporation
PARA-OXALOTOLUIDIDE 95.00%
5MG
$ 497.08

Total 6 raw suppliers

Chemical Property of p-Oxalotoluidide Edit

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：58.20000
Density:1.241g/cm³
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:306

Purity/Quality:

99% ^*data from raw suppliers

p-Oxalotoluidide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)NC(=O)C(=O)NC2=CC=C(C=C2)C
Uses A N,N’-diarylalkanediamide A N,N’-diarylalkanediamide having antimycobacterial and antialgal activity. A new group of potential tuberculostatics.

Technology Process of p-Oxalotoluidide

There total 23 articles about p-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:

Reference yield: 90.0%

: 79-37-8
oxalyl dichloride

: 6639-47-0
1,3,5-tris(p-tolyl)hexahydro-s-triazine

: 3299-61-4
N,N'-Di-p-tolyloxalamide

: 1,3-Di-p-tolyl-imidazolidine-4,5-dione

Guidance literature:: In diethyl ether; at 0 ℃; for 0.166667h;
DOI:10.1016/S0040-4020(01)81552-0

Reference yield: 90.0%

: 106-49-0,12221-03-3
p-toluidine

: 189274-63-3
7-Methyl-oxazolo[3,2-a]quinoline-1,2,5-trione

: 1677-44-7
4-hydroxy-6-methylquinolin-2(1H)-one

: 3299-61-4
N,N'-Di-p-tolyloxalamide

Guidance literature:: In acetone; for 2h;
DOI:10.1080/00304949709355186

Reference yield: 82.0%

: 622-58-2,374675-64-6
p-Tolylisocyanate

: 3299-61-4
N,N'-Di-p-tolyloxalamide

Guidance literature:: With N,N,N,N,N,N-hexamethylphosphoric triamide; samarium diiodide; In tetrahydrofuran; for 2.5h; Ambient temperature;
DOI:10.1246/cl.1992.1143