180033
4-Methoxy-N-methylaniline
98%
Synonym(s):
N-Methyl-p-anisidine
Sign Into View Organizational & Contract Pricing
All Photos(2)
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
Recommended Products
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
Looking for similar products? Visit Product Comparison Guide
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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
230.0 °F - closed cup
Flash Point(C)
110 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service