-0.79
Fenta Nyl
Mar 21, 2014
Jan 1, 1970(56y)
Jan 1, 2027(135d)
Combat
Kills92
Losses22
Efficiency81%
ISK
Destroyed26.82b
Lost447.37m
ISK Eff.98%
Solo
Solo Kills0
Solo Ratio0%
Final Blows4
Points92
Other
NPC Losses0
NPC Loss Ratio0%
Avg Kills/Day0.00
ActivityInactive
Minmatar
Sebiestor
-0.79
Fenta Nyl
Last Active
Mar 21, 2014
Birthday
Jan 1, 1970 (56 years old)
Next Birthday
Jan 1, 2027 (135 days)
Combat
Kills92
Losses22
Efficiency81%
Danger Ratio100%
ISK
Destroyed26.82b
Lost447.37m
ISK Efficiency98%
Balance+26.37b
Solo
Solo Kills0
Solo Ratio0%
Final Blows4
Points92
Other
NPC Losses0
NPC Loss Ratio0%
Avg Kills/Day0.00
ActivityInactive
Nothing in the last 7d
Bio
The synthesis of fenta nyl
(N-phenyl-N-(1-phenethyl-4-piperidinyl) propanamide) was achieved in four steps, starting from 4-piperidinone hydrochloride.
The 4-piperidinone hydrochloride was first reacted with phenethyl bromide to give N-phenethyl-4-piperidinone (NPP).
Treatment of the NPP intermediate with aniline followed by reduction with sodium borohydride afforded 4-anilino-N-phenethyl-piperidine (ANPP).
Finally ANPP and propionic anhydride are reacted to form the amide product.
(N-phenyl-N-(1-phenethyl-4-piperidinyl) propanamide) was achieved in four steps, starting from 4-piperidinone hydrochloride.
The 4-piperidinone hydrochloride was first reacted with phenethyl bromide to give N-phenethyl-4-piperidinone (NPP).
Treatment of the NPP intermediate with aniline followed by reduction with sodium borohydride afforded 4-anilino-N-phenethyl-piperidine (ANPP).
Finally ANPP and propionic anhydride are reacted to form the amide product.
Dashboard
Stats
No activity in the last 90d
Last seen Mar 2014
Intel Profile
PlaystyleSolo (0 kills)
Avg Fleet: -