I'm currently working with o-Phthalaldehyde (CAS: 643-79-8) and I am very interested in knowing the stability of this chemical. On the bottle is says that this chemical is "Air, light, temperature and moisture sensitive".
Have anybody synthesized acrylanilides? I would be very grateful for giving me any advices and sources about this topic. I'm making this synthesis from anhydrites and anilines, but I have problems with purifing these compounds. thanks in advance
Im taking med-chem and I was wondering if you had any suggestions to understanding some of the concepts. i.e. easy way to remember the Kreb cycle or the different uses for the many functional groups. thanks a bunch,
Can a Clemmensen reduction be used in this example to reduce the aldehyde group to methyl without affecting the double bond? R-CH=CH-CHO -> R-CH=CH-CH3 Thanks
first, I am sorry for my bad english, but however i hope that you understand my problem. Can anyone please sort the following molecules in their stability in the transition state (don't know if that is the right word), with the first number representing the most stabil carbokation. ...
I was wondering if anyone knows of a good experiment to do in a med chem class that deals with proteins or amino acids. I am looking for a synthisis, degradation, or extraction. I am open to any sugesstions or other possibilities.
I was going to synthesize some 7 substituted coumarins starting from 4-salicylaldehydes. The list of substituents would be chosen so that I would have a coumarin matching each benzene in the Johnson & Jankowski 13-C NMR catalog.
Would NBS react to monobrominate cyclopentane, and if so, what reaction conditions would be ideal? Chloroform, acetic anhydride, peroxides, intense light? Thank You to all who respond!