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Indole from feces
[quote]I just want indole. Pure indole. Just to have it.[/quote]
If that's all you want, the ... |
19-5-2005 at 10:50
by: Nicodem |
Good Read: Trichloroisocyanuric Acid - A Safe and Efficient Oxidant
Organikum, thanks a lot sincerely. There were a few papers I did not have and some of them are reall ... |
18-5-2005 at 11:41
by: Nicodem |
Photo-Catalytic chlorination of Toluene...
[quote]I was unaware that anyone actually got the TCCA halogenation to work... [/quote]
Off course ... |
16-5-2005 at 09:18
by: Nicodem |
How can someone be successful in Organic Chemistry?
In science we use theories in order to avoid using magic.
A theory is an explanation based on argum ... |
11-5-2005 at 13:48
by: Nicodem |
Theoretical Synthesis of 3,4,5-Alkoxy-PEA
PainKilla, it's true, there is nothing better than libraries to search for journal papers. The ... |
7-5-2005 at 01:01
by: Nicodem |
Theoretical Synthesis of 3,4,5-Alkoxy-PEA
Kyanite, mescaline has no chiral centers and hence no enantiomers. Neither does tyramine, so the chi ... |
6-5-2005 at 01:25
by: Nicodem |
adulteration of acid
Hm... sorry, my mistake.
Yes, potassium bisulphate is KHSO4. I got confused as I saw no reason on ... |
27-3-2005 at 09:52
by: Nicodem |
adulteration of acid
OK, I guess what works for sodium bisulphate works with potassium bisulphate as well, hence this rep ... |
27-3-2005 at 09:26
by: Nicodem |
Controlling Monomethylation of Hydroquinone to p-methoxyphenol
OK, it is true that the monomethylation of hydroquinone yields a dirty product which needs to be vac ... |
16-3-2005 at 09:49
by: Nicodem |
R-OH to R-leaving group?
Well, this was surely discussed a lot. But what exactly are you more interested in? How to put a lea ... |
8-3-2005 at 03:00
by: Nicodem |
Oxydation of Ethylamine into Nitroethane?
As already briefly mentioned by Kinetic, there is also another efficient OTC oxime-to-nitro oxidant, ... |
8-3-2005 at 02:46
by: Nicodem |
HCl and Al, AlCl3?
If I would be in a desperate need of anhydrous AlCl3 and only had OTC chemicals, I would try to make ... |
7-3-2005 at 08:07
by: Nicodem |
Al/Hg Reduction & Dehalogenation.
Off course you can. Al-Hg reduction does not dehalogenate haloaromatics.
Don't expect 3-Br-4-M ... |
2-3-2005 at 09:58
by: Nicodem |
toluene oxidation fun
I doubt you can make benzaldehyde using persulphates, H2O2 with catalysts or other such oxidants in ... |
20-2-2005 at 12:39
by: Nicodem |
From Anise Star to Mescaline.
Sparkgap, I'm convinced that anethole can be brominated twice on the ring plus on the side chai ... |
11-2-2005 at 11:39
by: Nicodem |
From Anise Star to Mescaline.
I find it impossible that you can doubly brominate anethole without brominating the double bond as w ... |
11-2-2005 at 11:24
by: Nicodem |
Why DNA?
Those amino groups on adenine, cytosine and guanine are very weak bases. These amino functions are e ... |
8-2-2005 at 11:45
by: Nicodem |
chlorosulfonylation
The electron withdrawing character of Cl makes the Cl-SO2+ electrophyle more reactive than HO-SO2+ ... |
7-2-2005 at 10:07
by: Nicodem |
Dillute DMSO with water
The standard method is to dillute the DMSO solution with water and then extract with a non-polar sol ... |
14-1-2005 at 05:30
by: Nicodem |
