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Bromine Source and Synthesis
what reaction does it produce: NaBrO3 + Cl2 =>? |
15-1-2007 at 09:17
by: Filemon |
Bromine Source and Synthesis
That solubility has in water ClBr? |
14-1-2007 at 04:38
by: Filemon |
Bromine Source and Synthesis
[quote][i]Originally posted by PainKilla[/i]
Trichloroisocyanuric acid is a most excellent source o ... |
7-1-2007 at 10:43
by: Filemon |
Bromine Source and Synthesis
[quote][i]Originally posted by evil_lurker[/i]
BCDMH is definately an interesting chemical and a da ... |
4-1-2007 at 15:52
by: Filemon |
Chlorination with CuCl2
How is the reaction?
Acetone + 2 CuCl2 => chloroacetone + 2 CuCl + HCl? |
27-11-2006 at 05:53
by: Filemon |
Al + NH4Cl
What does it take place reaction? Al + NH4Cl => AlCl3 + NH3 + H2? |
30-9-2006 at 14:49
by: Filemon |
Friedel-Crafts alkylation with FeCl3
Thank. I already know the theory. For this reason I have doubts about the effectiveness of this meth ... |
19-9-2006 at 14:09
by: Filemon |
Friedel-Crafts alkylation with FeCl3
Does it have good yield the Friedel-Crafts alkylation with FeCl3 and chloroacetone?
Edit by Chemo ... |
19-9-2006 at 09:08
by: Filemon |
Mechanism REDOX sugar + KNO3?
How is the reaction sugar + KNO3 =>? |
31-8-2006 at 11:43
by: Filemon |
Amphetamine from Cinnamaldehyde
here => http://www.chem.harvard.edu/groups/myers/handouts/1_Reduction.pdf
pg.7
http://en.wi ... |
5-8-2006 at 13:10
by: Filemon |
Amphetamine from Cinnamaldehyde
I have in mind to use the Wolff-Kisher Reduction:
ph-CH=CH-CH=O + NH2-NH2 => PH-CH=CH-CH=N-NH2 ... |
5-8-2006 at 11:16
by: Filemon |
Amphetamine from Cinnamaldehyde
[quote][i]Originally posted by Vitus_Verdegast[/i]
Be aware that in most countries it is a felo ... |
5-8-2006 at 10:51
by: Filemon |
Amphetamine from Cinnamaldehyde
I was thinking to make amphetamine from Cinnamaldehyde:
1. - Cinnamaldehyde + HCl--> 3-Phe ... |
4-8-2006 at 12:18
by: Filemon |
Acid-catalysed halogenation
Excuse me. I have mistake. A strong acid is a catalyzed best. |
26-7-2006 at 15:00
by: Filemon |
Acid-catalysed halogenation
I believe that you have mistake. I'm not speaking acetic acid halogenation but acetone. |
26-7-2006 at 14:24
by: Filemon |
Acid-catalysed halogenation
I want to make iodoacetone:
acetone + I2---H+--> iodoacetone + ... |
26-7-2006 at 11:46
by: Filemon |
[edit]
[quote][i]Originally posted by Organikum[/i]
H2SO4 if not very diluted oxidizes HI.
[Edited on ... |
25-7-2006 at 04:31
by: Filemon |
Enolate Alkylation
Where I can find it? I have not found it in internet. |
24-7-2006 at 02:45
by: Filemon |
Enolate Alkylation
t-BuONa is sufficiently strong? |
23-7-2006 at 15:51
by: Filemon |
Enolate Alkylation
An enolate preparation needs low temperatures. Why? if it was made to bigger temperatures that it wo ... |
19-7-2006 at 08:15
by: Filemon |
Urushibara Catalysts
Does the Urushibara reduce imine?
[Edited on 16-7-2006 by Filemon] |
16-7-2006 at 14:00
by: Filemon |
Physical properties of Phenylpropanolamine?
Thanks  |
6-7-2006 at 02:25
by: Filemon |
Physical properties of Phenylpropanolamine?
I need to know mp Phenylpropanolamine base and other physical properties. |
5-7-2006 at 12:10
by: Filemon |
Dimenoxadol
I want an analgesic effective but it isn't necessary very potent. I have chosen Dimenoxadol. I have ... |
23-5-2006 at 15:35
by: Filemon |
Amphetamine via ephedrine?
Is it possible to synthesize amphetamine with the method of Urushibara?
Ephedrine =======> ... |
26-4-2006 at 15:06
by: Filemon |
