I don't love the name 'CanKet' mostly because it's misleading.
Ketamine is
3-Chloro-2'-Oxo-PCM, right? And if you remove the chlorine atom you get
deschloroketamine (DCK). Put a fluorine atom on the 2-position and you've got
2F-DCK which is also called
O-PCM. In my mind, these are ketamine-class drugs, defined by the double-bond oxygen on the cyclohexyl ring + a single-carbon methyl group – the source of the M in
O-PCM. If instead of the methyl group, one makes that a two-carbon ethyl chain, we arrive at the drug
O-PCE. Now we've got the scaffold for what I think of as "__oxetamine"-class drugs. This includes
MXE,
FXE, and
HXE among others.
From this nomenclature we could choose to think of Ketamine-class drugs as "__ox
metamine"-class drugs, though this is admittedly a bit confusing if you're not paying close attention. And let's say you remove everything from the nitrogen (the amino functional group). This would be
deschloronorketamine or DCNK.
Clear as mud?
Me, too! Also, 3-HO-PCP, which I might even prefer at times to 3-MeO-PCP, though they're both similar to one another and to PCP…
It does? I think you might need to seek new sources then… Compared to other drugs, designer dissos are somewhat rare and rather niche in terms of popularity. Most ppl avoid dissos with the exception of Ketamine, mostly I think owing to the bad reputation PCP has garnered over the years. But if you know where to look, they abound. In certain circles, designer dissos are all over the place, and there are a metric
shit ton of them.
That's correct, 2-Fluoro-O-PCE, aka "
n-ethyl-2FDCK". And in my mind, given that FXE is 3-Fluoro-2'-Oxo-PCE, the nickname I prefer for what has been labelled Can-Ket is 2FXE, and what's called FXE could be called 3-FXE to distinguish them. Purportedly 5-FXE is a worthwhile compound, too. I guess alternatively we could call 3-FXE "meta-FXE", which would make 2-FXE "ortho-FXE" and by extension, 4-FXE would be "para-FXE"… Ow, I think my brain hurts now, lol
Um… yeahhh, no. It doesn't really hold up to PCP. It has more in common with Ketamine and MXE than it does PCP and its 3-oxygen-moiety-substituted analogs (e.g.: 3-MeO-PCP, 3-HO-PCP). Generally I feel like dissos are either stimulating or sedating – e.g. Ketamine is sedating while PCP is stimulating. 2FXE is of the sedating variety. I was expecting it to be more like MXE and found myself disappointed when it came up short, so I shelved it for months until a friend asked me to try it. He loved it and it convinced me to re-appraise it, this time with lower expectations. I was pleasantly surprised that it's got its own charms and I consider the compound worthy of exploration. Higher doses can become mystical, even.
Hmmm, that's a bit subjective and hard to say; also depends on how you define mania. I think probably yes, just not as profoundly and easily as PCP and its close analogs. What's good about those drugs is they're so potent the average dose is quite small and this limits its potentially to damage the bladder as most of these dissos have the capability to do if abused. So something that's active @ 50 mg is going to deal out more damage potentially than something that's active around 8 mg just by sheer logistics and surface area geometry. Also, keep in mind that mania can be a dual-edged sword, so to speak. Mania is disinhibiting, and when inhibition is lowered, shit crappens.
It mixes really well w/psychedelics, in my opinion, and that's using it before, during, and after the trip. On separate occasions I've mixed it with LSD, DMT, Psilacetin, Colour, 2C-B, Allylescaline, and 25B-NBOH all with much success. It's not a show stopper, 2FXE, not the main course entree for the evening, as it were, but it's definitely a 'tasty' little tapas a la carte drug with the ability to pique a psychedelic experience / entheogen session. In summary, keep your expectations low and you might be pleasantly surprised. At least, that was my experience and proverbial $0.02. YMMV, and good luck! Hope this helps