-0.79
Fenta Nyl
Mar 21, 2014
Jan 1, 1970(56y)
Jan 1, 2027(199d)
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 (199 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
No data available
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
Kills0
Losses0
Efficiency0%
ISK Destroyed0
ISK Lost0
ISK Efficiency0%
Solo Kills0
Solo Losses0
NPC Losses0
Blob Factor0
Active TimezoneUSTZ
Final Blows0
Points0
Activity Heat Map (EVE Time)
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Intel Profile
PlaystyleSolo (0 kills)
Avg Fleet: -