180033
4-Methoxy-N-methylaniline
98%
Synonym(s):
N-Methyl-p-anisidine
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About This Item
Linear Formula:
CH3OC6H4NHCH3
CAS Number:
Molecular Weight:
137.18
Beilstein:
774640
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
98%
form
solid
bp
135-136 °C/19 mmHg (lit.)
mp
33-36 °C (lit.)
SMILES string
CNc1ccc(OC)cc1
InChI
1S/C8H11NO/c1-9-7-3-5-8(10-2)6-4-7/h3-6,9H,1-2H3
InChI key
JFXDIXYFXDOZIT-UHFFFAOYSA-N
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General description
The allylation of N-methyl-p-anisidine by quaternary allylammonium cation was studied.
Application
4-Methoxy-N-methylaniline (N-Methyl-p-anisidine) was used to study the additive effects of amines.
WGK
WGK 3
Flash Point(F)
230.0 °F
Flash Point(C)
110 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Andrea Cappelli et al.
Bioorganic & medicinal chemistry, 16(6), 3428-3437 (2008-02-26)
The exploration of the structure-affinity relationships concerning a new class of peripheral benzodiazepine receptor (PBR) ligands related to alpidem has been pursued in order to evaluate the consistency of the structure-affinity relationships among different classes (and subclasses) of PBR ligands.
Takuto Nagano et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(37), 11578-11592 (2012-08-24)
The additive effects of amines were realized in the asymmetric hydrogenation of 2-phenylquinoxaline, and its derivatives, catalyzed by chiral cationic dinuclear triply halide-bridged iridium complexes [{Ir(H)[diphosphine]}(2)(μ-X)(3)]X (diphosphine = (S)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl [(S)-BINAP], (S)-5,5'-bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole [(S)-SEGPHOS], (S)-5,5'-bis(diphenylphosphino)-2,2,2',2'-tetrafluoro-4,4'-bi-1,3-benzodioxole [(S)-DIFLUORPHOS]; X = Cl, Br, I) to
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