N-Methylfentanyl

Base Information

Chemical Name:N-Methylfentanyl
CAS No.:22261-99-0
Molecular Formula:C₁₅H₂₂N₂O
Molecular Weight:246.352
Hs Code.:
UNII:HOA9FEV2M0
DSSTox Substance ID:DTXSID50335758
Nikkaji Number:J1.129.880J,J470.601C
Wikidata:Q27130741
Metabolomics Workbench ID:61460
ChEMBL ID:CHEMBL170779

Synonyms:N-Methylfentanyl;N-methylfentanil;N-Methylnorfentanyl;Methyl norfentanyl;22261-99-0;N-(1-methylpiperidin-4-yl)-N-phenylpropanamide;HOA9FEV2M0;Propanamide, N-(1-methyl-4-piperidinyl)-N-phenyl-;CHEBI:61102;UNII-HOA9FEV2M0;1-Methyl-4-(N-phenylpropionamido)piperidine;N-(1-Methyl-4-piperidinyl)-N-phenylpropanamide;N-(1-Methyl-4-piperidyl)-N-phenyl-propanamide;Epitope ID:153517;N-METHYL NORFENTANYL;CHEMBL170779;SCHEMBL5164451;DTXSID50335758;N-METHYL NORFENTANYL [NFLIS-DRUG];1-methyl-4-(N-propionylphenylamino)-piperidine;N-Phenyl-N-(1-methyl-4-piperidinyl)propanamide;Q27130741

Suppliers and Price of N-Methylfentanyl

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

Total 0 raw suppliers

Chemical Property of N-Methylfentanyl

Chemical Property:

PSA：23.55000
LogP:2.46170
XLogP3:2.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:246.173213330
Heavy Atom Count:18
Complexity:266

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC(=O)N(C1CCN(CC1)C)C2=CC=CC=C2

Technology Process of N-Methylfentanyl

There total 1 articles about N-Methylfentanyl 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: 86.0%

: 22261-99-0
N-(1-methyl-piperidin-4-yl)-N-phenyl-propionamide

Guidance literature:

Reference yield:

: 22261-99-0
N-(1-methyl-piperidin-4-yl)-N-phenyl-propionamide

: 85893-35-2
N-(1-Methyl-1-oxy-piperidin-4-yl)-N-phenyl-propionamide

Guidance literature:: With dihydrogen peroxide; In methanol; 1.) room temperature, 48 h, 2.) heating, 2 h; other reagent: m-chloroperbenzoic acid;

Reference yield:

: 22261-99-0
N-(1-methyl-piperidin-4-yl)-N-phenyl-propionamide

: N-(2-cyano-1-methyl-4-piperidino)-N-phenylpropane amide

Guidance literature:: Multi-step reaction with 2 steps

1: aq. hydrogen peroxide / methanol / 1.) room temperature, 48 h, 2.) heating, 2 h; other reagent: m-chloroperbenzoic acid

2: 1.) trifluoroacetic anhydride / 1.) methylene chloride, room temperature, 1 h; heating, 20 min, 2.) water, room temperature, 1 h

With dihydrogen peroxide; trifluoroacetic anhydride; In methanol;