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ALD-52 vs. LSD-25
Aye, I was wondering if anyone could help me out on this, I'm sorry if
my question seems stupid but I can't seem to find any good resources on Organic chemistry, and I don't know how the damn carbon rings are numbered (neither do my chem teachers lol). ALD-52 differs from LSD-25 in that at N-1 there is a COCH3 connected to the pyrrole ring as apposed to a single Hydrogen (found in LSD-25). ![]() This is fine but by definition the pyrrole ring is a heterocyclic ring of C4H5N, and the only Hydrogen connected at a Nitrogen is near the bottom (of the picture). But that is not a pyrolle ring. Supposedly the double bonds between the carbons act as a Hydrogen but that would only make up 4 if my math is right. Meaning C4H4N. How would that be possible? Is that were theCOCH3 connects? Im not sure if I should even bother with it. Some people say ALD-52 is better than LSD but others disagree. I havent had the pleasure to synthesis or try either
Last edited by Jatelka; 29-09-2007 at 09:53. Reason: code removal |
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