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β-Phenylmethamphetamine

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(Redirected from Beta-Phenylmethamphetamine)
β-Phenylmethamphetamine
Clinical data
ATC code
  • none
Legal status
Legal status
  • DE: NpSG (Industrial and scientific use only)
  • UK: Class A
Identifiers
  • 1,1-diphenyl-2-methylaminopropane
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC16H19N
Molar mass225.335 g·mol−1
3D model (JSmol)
  • c2ccccc2C(C(C)NC)c1ccccc1
  • InChI=1S/C16H19N/c1-13(17-2)16(14-9-5-3-6-10-14)15-11-7-4-8-12-15/h3-13,16-17H,1-2H3
  • Key:YZFPOMOQFPMBPK-UHFFFAOYSA-N
  (verify)

β-Phenylmethamphetamine (N,α-dimethyl-β-phenyl-phenethylamine) is a potent and long lasting stimulant drug.[1][2]

Synthesis

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1,1-Diphenylacetone is also used in the synthesis of Diphenadione.

1,1-diphenylacetone synthesis:[3][4][5]

See also

[edit]

References

[edit]
  1. Heinzelman RV (February 1953). "Physiologically active secondary amines. β-(o-Methoxyphenyl)-isopropyl-N-methylamine and related compounds". Journal of the American Chemical Society. 75 (4): 921–5. doi:10.1021/ja01100a043.
  2. Schmidt D, Hüller H, Amon I, Peters R (October 1973). "[On the pharmacology of a series of diphenylaminopropane derivatives]". Die Pharmazie (in German). 28 (10): 677–80. PMID 4783556.
  3. α,α-DIPHENYLACETONE, Everett M. Schultz and Sally Mickey, Org. Synth. 1949, 29, 38, DOI: 10.15227/orgsyn.029.0038.
  4. Mukaiyama, T., Echigo, Y., Shiono, M. (5 February 1977). "A FACILE METHOD FOR THE PINACOL REARRANGEMENT OF PHENYLETHANEDIOL DERIVATIVES BY THE USE OF 2-CHLOROPYRIMIDINIUM SALT". Chemistry Letters. 6 (2): 179–180. doi:10.1246/cl.1977.179.
  5. Posner, G. H., Whitten, C. E. (January 1970). "Methyl and -alkyl ketones from carboxylic acid chlorides and organocopper reagents". Tetrahedron Letters. 11 (53): 4647–4650. doi:10.1016/S0040-4039(00)89398-3.