2-Phenylethylamine

• Catalog No.: A13402
• CAS Number: 64-04-0
• M. F.: C8H11N
• M. W.: 121.17964
• Purity: 99%

SYNONYMS

• Title: 2-苯基乙胺
• IUPAC name: 2-phenylethan-1-amine
• IUPAC Traditional name: 2-phenylethylamine
• Synonyms: (2-Aminoethyl)benzene; Phenethylamine

DATABASE IDS

• Beilstein Number: 507488
• MDL Number: MFCD00008184
• Merck Index: 147225
• CAS Number: 64-04-0
• EC Number: 200-574-4

PROPERTIES

• RTECS: SG8750000
• Safety Statements: 26-36/37/39-45
• Storage Warning: Air Sensitive
• TSCA Listed: 是
• Hazard Class: 8
• UN Number: UN2922
• Packing Group: II
• GHS Hazard statements: H301-H314-H318-H227
• European Hazard Symbols: X
• European Hazard Symbols: Corrosive (C)
• GHS Precautionary statements: P210-P301+P310-P303+P361+P353-P305+P351+P338-P405-P501A
• Risk Statements: 22-34
• Purity: 99%
• Boiling Point: 200-202°C
• Density: 0.964
• Flash Point: 81°C(178°F)
• Melting Point: -60°C
• Refractive Index: 1.5335

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).