Mebenil

Base Information

Chemical Name:Mebenil
CAS No.:7055-03-0
Molecular Formula:C14H13NO
Molecular Weight:211.263
Hs Code.:
European Community (EC) Number:230-334-4
NSC Number:227402,26404
UNII:B8MA40FMWG
DSSTox Substance ID:DTXSID5042116
Nikkaji Number:J8.888I
Wikidata:Q27155712
ChEMBL ID:CHEMBL1328781
Mol file:7055-03-0.mol

Synonyms:2-toluanilide;o-toluanilide

Suppliers and Price of Mebenil

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

Usbiological
o-Toluanilide
100mg
$ 305.00

TRC
o-Toluanilide
500mg
$ 125.00

Sigma-Aldrich
O-TOLUANILIDE Aldrich
250mg
$ 33.40

Oakwood
2-Methyl-N-phenylbenzamide 98%
250mg
$ 75.00

American Custom Chemicals Corporation
2-METHYL-N-PHENYLBENZAMIDE 95.00%
5MG
$ 497.50

AHH
2-Toluanilide 98%
10g
$ 820.00

Total 11 raw suppliers

Chemical Property of Mebenil

Chemical Property:

Vapor Pressure:0.00483mmHg at 25°C
Refractive Index:1.5780 (estimate)
Boiling Point:276.3oC at 760 mmHg
PKA:13.53±0.70(Predicted)
Flash Point:162.2oC
PSA：29.10000
Density:1.144g/cm3
LogP:3.32030
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:211.099714038
Heavy Atom Count:16
Complexity:233

Purity/Quality:

99.0% ^*data from raw suppliers

o-Toluanilide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=CC=C1C(=O)NC2=CC=CC=C2
Uses o-Toluanilide is a systemic fungicide used in pesticide formulations.

Technology Process of Mebenil

There total 71 articles about Mebenil 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: 100.0%

: 933-88-0
ortho-toluoyl chloride

: 62-53-3
aniline

: 7055-03-0
2-methyl-N-phenylbenzamide

Guidance literature:: In diethyl ether; Ambient temperature;
DOI:10.1007/BF00799564

Reference yield: 99.0%

: 118-90-1
ortho-methylbenzoic acid

: 62-53-3
aniline

: 7055-03-0
2-methyl-N-phenylbenzamide

Guidance literature:: ortho-methylbenzoic acid; With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 0.166667h; Inert atmosphere;

aniline; With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 60 ℃; Inert atmosphere;
DOI:10.1021/jm500191u

Reference yield: 97.0%

: 15813-38-4
phenyl 2-methylbenzoate

: 62-53-3
aniline

: 7055-03-0
2-methyl-N-phenylbenzamide

Guidance literature:: With [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium carbonate; In 1,2-dimethoxyethane; at 110 ℃; for 16h; Inert atmosphere; Schlenk technique;
DOI:10.1039/c7cc06186b