N,N-Dimethyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenamine

Base Information

Chemical Name:N,N-Dimethyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenamine
CAS No.:118183-93-0
Molecular Formula:C₁₁H₁₃N₃O
Molecular Weight:203.244
Hs Code.:
DSSTox Substance ID:DTXSID201195313

Synonyms:SCHEMBL19080652;DTXSID201195313;N,N-Dimethyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenamine;118183-93-0

Suppliers and Price of N,N-Dimethyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenamine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of N,N-Dimethyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenamine

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:203.105862047
Heavy Atom Count:15
Complexity:202

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=NC(=NO1)C2=CC=C(C=C2)N(C)C

Technology Process of N,N-Dimethyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenamine

There total 3 articles about N,N-Dimethyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenamine 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: 81.4%

: 68451-71-8,1585960-54-8
4-(dimethylamino)-N'-hydroxybenzimidamide

: 75-36-5
acetyl chloride

: 118183-93-0
3-(4-dimethylaminophenyl)-5-methyl-1,2,4-oxadiazole

Guidance literature:: In pyridine;

Reference yield:

: 1197-19-9
4-cyano-N,N-dimethylaniline

: 118183-93-0
3-(4-dimethylaminophenyl)-5-methyl-1,2,4-oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: hydroxylamine hydrochloride, sodium hydroxide / H₂O / 4 h / Heating

2: diphenyl ether / 125.3 °C

With sodium hydroxide; hydroxylamine hydrochloride; In diphenylether; water;
DOI:10.1039/P29800001792