Substance
ID:716318
Names and Identifiers
IUPAC Traditional name
2-phenylethylamine
IUPAC name
2-phenylethan-1-amine
Synonyms
2-Phenylethylamine2-苯基乙胺Phenethylamine(2-Aminoethyl)benzene
Registration numbers
EC Number
MDL Number
CAS Number
Beilstein Number
Merck Index
Properties
Product Information
Purity
99%
Physical Property
Flash Point
81°C(178°F)
Refractive Index
1.5335
Density
0.964
Boiling Point
200-202°C
Melting Point
-60°C
Safety Information
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
European Hazard Symbols
Harmful (X)
Corrosive (C)Packing Group
II
GHS Hazard statements
H301-H314-H318-H227
Storage Warning
Air Sensitive
RTECS
SG8750000
Safety Statements
26-36/37/39-45
UN Number
UN2922
Risk Statements
22-34
Hazard Class
8
GHS Precautionary statements
P210-P301+P310-P303+P361+P353-P305+P351+P338-P405-P501A
TSCA Listed
是
Molecule Details
No Data Available
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Molecular Spectra
No Data Available
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References
• N-Acyl-derivatives are cyclized by a variety of reagents, e.g. P2O5, POCl3, PCl5, etc., to derivatives of isoquinoline, in the Bischler-Napieralski synthesis. For a review, see: Org. React., 6, 74 (1951). Similarly, imines can be cyclized to derivatives of tetrahydroisoquinoline in the Pictet-Spengler synthesis. Reviews: Org. React., 6, 151 (1951); Adv. Het. Chem., 3, 79 (1964); Heterocycles, 3, 223 (1975); 39, 903 (1994).