This may appear a chem wank but I do have a few serious points so I am hoping it will be accepted:
1) Does anyone know if these have been investigated? (any info at all scientific or otherwise) It seems perfectly logical considering the dragonflys, flys, TCB-2 and recently read even a tryptamine have had their corresponding NBOMe's explored.
2) N-substitution was talked about a lot (I believe pre-NBOMe's) in reference to beta-ketones, I.e there was long discussion about how simple unsubstituted PEA's (e.g 2c-b) can not have their corresponding beta-ketone explored because without N-substitution they are very unstable and therefore problematic if not impossible. NBOMe's turn the annoying necessity of HAVING to have a N-substitution for stability in to actually optimising 5HT2a agonism etc.
3) Although not a viable scientific point, I would imagine the bk-NBOMes would be legal in many places as the corresponding PEA would not be a impurity (as has been found the case recently with normal NBOMe's). Anyone know if the (at present purely theoretical) bk-2-c-b is covered by UK cathinone catch'all?
It would also be of great interest to finally have a beta-ketone psychadelic analogue (if I am correct so far this has not occurred? The closest I am guessing is ecstasy type compounds lying somewhere in between stimulants and psychedelics i.e methylone/methylmethcathinone etc etc)
1) Does anyone know if these have been investigated? (any info at all scientific or otherwise) It seems perfectly logical considering the dragonflys, flys, TCB-2 and recently read even a tryptamine have had their corresponding NBOMe's explored.
2) N-substitution was talked about a lot (I believe pre-NBOMe's) in reference to beta-ketones, I.e there was long discussion about how simple unsubstituted PEA's (e.g 2c-b) can not have their corresponding beta-ketone explored because without N-substitution they are very unstable and therefore problematic if not impossible. NBOMe's turn the annoying necessity of HAVING to have a N-substitution for stability in to actually optimising 5HT2a agonism etc.
3) Although not a viable scientific point, I would imagine the bk-NBOMes would be legal in many places as the corresponding PEA would not be a impurity (as has been found the case recently with normal NBOMe's). Anyone know if the (at present purely theoretical) bk-2-c-b is covered by UK cathinone catch'all?
It would also be of great interest to finally have a beta-ketone psychadelic analogue (if I am correct so far this has not occurred? The closest I am guessing is ecstasy type compounds lying somewhere in between stimulants and psychedelics i.e methylone/methylmethcathinone etc etc)
