Fencamfamine
Title: Fencamfamine
CAS Registry Number: 1209-98-9
CAS Name: N-Ethyl-3-phenylbicyclo[2.2.1]heptan-2-amine
Additional Names: N-ethyl-3-phenyl-2-norbornanamine; 2-ethylamino-3-phenylnorcamphane; 2-phenyl-3-ethylaminonorbornane; 2-ethylamino-3-phenylnorbornane; 2-ethylamino-3-phenylbicyclo[2.2.1]heptane
Trademarks: Euvitol (Allen & Hanburys)
Molecular Formula: C15H21N
Molecular Weight: 215.33
Percent Composition: C 83.67%, H 9.83%, N 6.50%
Literature References: Prepd from 3-amino-2-phenylnorbornane and acetaldehyde followed by hydrogenation in the presence of PtO2: Thesing et al., DE 1110159 (1961 to E. Merck), C.A. 56, 2352g (1962). Pharmacology: R. Hotovy et al., Arzneim.-Forsch. 11, 20 (1961).
Properties: bp0.1 128-131°.
Boiling point: bp0.1 128-131°
 
Derivative Type: Hydrochloride
CAS Registry Number: 2240-14-4
Manufacturers' Codes: H-610
Molecular Formula: C15H21N.HCl
Molecular Weight: 251.79
Percent Composition: C 71.55%, H 8.81%, N 5.56%, Cl 14.08%
Literature References: Principal ingredient of Reactivan (Cascan) which also contains vitamins B1, B6, B12 and C.
Properties: Crystals from acetone, mp 192°. Freely sol in water, ethanol, methanol, chloroform; slightly sol in benzene. Practically insol in ether. LD50 in mice, rats (mg/kg): 135.0, 113.0 orally; 85.5, 68.5 s.c.; 15.7, 23.5 i.v. (Hotovy).
Melting point: mp 192°
Toxicity data: LD50 in mice, rats (mg/kg): 135.0, 113.0 orally; 85.5, 68.5 s.c.; 15.7, 23.5 i.v. (Hotovy)
 
NOTE: This is a controlled substance (stimulant): 21 CFR, 1308.14.
Therap-Cat: CNS stimulant.
Keywords: CNS Stimulant.

Others monographs:
MoxalactamEtamycinLBFn-Butyl Carbonate
Vanilmandelic AcidBeractantTiaramideBeryllium Sulfate
BumetanideNalidixic AcidUricaseCyclobuxine D
Alcian BlueTebufenpyrad1-Phenyl-3-pyrazolidinoneMethyl Chlorocarbonate
©2016 DrugLead US FDA&EMEA