Dr.Heckyll
Bluelighter
- Joined
- Sep 16, 2006
- Messages
- 138
Do you have a reference for this?
N&PD Moderators: Skorpio | someguyontheinternet
Dr.Heckyll said:Do you have a reference for this?
A general organic chem blonde question: How difficult is it in general to nitrogenate an aromatic ring?
I suspect that what he is asking is whether nitrogen can be inserted into the benzene ring as part of the ring... benzene to pyridine, or naphthaline to quinoline, which is what is required to convert the NSAI into AFA. this is essentially impossible.phase_dancer said:Basically aromatic + HNO3/H2SO4, although if other ring substitutes are present, depending upon whether they are activating or deactivating, the Nitro group will either be directed to para/ ortho or meta positions.
jah said:Yes it does, F&B and Dr.Heckyll both had really good things to say about it. Maybe this guy wasn't to far off the mark!!!
Thanks.
The structure reminds me very, very much of gyrase inhibitors such as enoxycin or ciproflixacin. I am pretty sure amfonelic acid was originally synthesized as an antibiotic compound.
fastandbulbous said:That's the one thing that really worries me about AFA - if it has significant antibiotic activity, repeated, irregular use could lead to development of very nasty strains of normal body flora, the ones to really worry about being the opportune pathogens (like Staph. aureus) or could sizably upset the gut's normal flora leading to all manner of digestive tract problems.
In the meantime I had the opportunity to try foxolinic acid. It's a powerful and long lasting (~24h) stimulant at a dose of 5mg in some people, while others show little response to it. Like with AFA, there's no body lead at all, but AFA is more euphorigenic, lasts shorter and is more reliable. AFA is clearly the better choice. AFA is the absolutely best stimulant I've ever had, and I've had quite a few. Compared to AFA, MDPV is just shit which you wouldn't touch again if you had the choice. source discussion removedDr.Heckyll said:There's a related compound, Foxolinic Acid, which is about 4 times as potent as Amfonelic acid, and I've heard that some people are working on bringning that out on the market. That will be the end of MDPV i guess...