270229
3-Methoxyphenethylamine
97%
Synonym(s):
2-(3-Methoxyphenyl)ethylamine
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About This Item
Linear Formula:
CH3OC6H4CH2CH2NH2
CAS Number:
Molecular Weight:
151.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-017-9
Beilstein/REAXYS Number:
775202
MDL number:
Assay:
97%
Form:
liquid
InChI key
WJBMRZAHTUFBGE-UHFFFAOYSA-N
InChI
1S/C9H13NO/c1-11-9-4-2-3-8(7-9)5-6-10/h2-4,7H,5-6,10H2,1H3
SMILES string
COc1cccc(CCN)c1
assay
97%
form
liquid
refractive index
n20/D 1.538 (lit.)
bp
118-119 °C/6 mmHg (lit.)
density
1.038 g/mL at 25 °C (lit.)
functional group
amine
Quality Level
Related Categories
General description
The spectral binding affinity for 3-methoxyphenethylamine was studied to examine the determinants of P450 2D6 catalysis.
Application
3-Methoxyphenethylamine was used in the perfluorooctanesulfonic acid catalyzed Pictet-Spengler reaction. It was also used in the synthesis of 1,3-oxazepines via palladium-catalyzed intramolecular coupling.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Tetrahedron Letters, 48, 835-835 (2007)
P T Wong et al.
Neuroreport, 5(1), 53-56 (1993-10-25)
The effects of death and various treatments that affect the status of nigrostriatal neurones on striatal release of dopamine (DA) and 5-hydroxytryptamine (5-HT) and their metabolites 3,4-dihydroxyphenylacetic acid (DOPAC), 3-methoxy-4-hydroxyphenylethylamine (3-MT), homovanillic acid (HVA) and 5-hydroxyindoleacetic acid (5-HIAA) were studied
Tetrahedron, 62, 9002-9002 (2006)
G P Miller et al.
Biochemistry, 40(47), 14215-14223 (2001-11-21)
Cytochrome P450 (P450) 2D6 oxidizes a wide variety of drugs typically at a distance of 5-7 A from a basic nitrogen on the substrate. To investigate the determinants of P450 2D6 catalysis, we analyzed the binding and oxidation of phenethylamine
Anita H Lewin et al.
Bioorganic & medicinal chemistry, 16(15), 7415-7423 (2008-07-08)
A cell line in which RD-HGA16 cells were stably transfected with the hTAAR 1 receptor was created and utilized to carry out a systematic evaluation of a series of beta-phenethylamines. Fair agreement was observed with data obtained for aryl and
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