n-Methyl-4-(trifluoromethyl)benzamide

Base Information

Chemical Name:n-Methyl-4-(trifluoromethyl)benzamide
CAS No.:65017-76-7
Molecular Formula:C9H8F3NO
Molecular Weight:203.164
Hs Code.:
ChEMBL ID:CHEMBL4087004
DSSTox Substance ID:DTXSID70569412
Nikkaji Number:J3.212.191H

Synonyms:n-methyl-4-(trifluoromethyl)benzamide;65017-76-7;SCHEMBL3655196;CHEMBL4087004;DTXSID70569412;n-methyl-4-trifluoromethyl-benzamide;MFCD19595561;AKOS008932986;SB77404;Benzamide, 4-(trifluoromethyl)-N-methyl-;G66070

Suppliers and Price of n-Methyl-4-(trifluoromethyl)benzamide

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 4 raw suppliers

Chemical Property of n-Methyl-4-(trifluoromethyl)benzamide

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:203.05579836
Heavy Atom Count:14
Complexity:207

Purity/Quality:: 98%+ ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CNC(=O)C1=CC=C(C=C1)C(F)(F)F

Technology Process of n-Methyl-4-(trifluoromethyl)benzamide

There total 17 articles about n-Methyl-4-(trifluoromethyl)benzamide 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: 93.0%

: 116332-61-7
N-methoxy-N-methyl-4-trifluoromethylbenzamide

: 65017-76-7
N-methyl-4-(trifluoromethyl)benzamide

Guidance literature:: With o-phenylenebis(diphenylphosphine); triisobutylaluminum; bis(dibenzylideneacetone)-palladium⁽⁰⁾; In hexane; at 150 ℃; for 6h; chemoselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1039/d0ob01815e

Reference yield: 86.0%

: 67-56-1
methanol

: 66046-34-2
4-(trifluoromethyl)benzaldehyde oxime

: 65017-76-7
N-methyl-4-(trifluoromethyl)benzamide

Guidance literature:: With C₅₄H₄₃ClN₃P₂Ru⁽¹⁺⁾*F₆P^(1-); caesium carbonate; In toluene; at 140 ℃; for 24h; Inert atmosphere; Schlenk technique; Green chemistry;
DOI:10.1002/adsc.201900962

Reference yield: 84.0%

: 67-56-1
methanol

: 1891-90-3
p-trifluoromethylbenzamide

: 65017-76-7
N-methyl-4-(trifluoromethyl)benzamide

Guidance literature:: With C₅₄H₄₃ClN₃P₂Ru⁽¹⁺⁾*F₆P^(1-); caesium carbonate; In toluene; at 140 ℃; for 24h; Inert atmosphere; Sealed tube; Green chemistry;
DOI:10.1021/acs.orglett.9b01925