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  1. Category. v. t. e. Organic chemistry is a subdiscipline within chemistry involving the scientific study of the structure, properties, and reactions of organic compounds and organic materials, i.e., matter in its various forms that contain carbon atoms. [1] Study of structure determines their structural formula.

  2. Mechanism: A detailed mechanism illustrating the conversion of an amine to amide 3- (ethyliminomethyleneamino)-N,N-dimethylpropan-1-amine (EDC) and hydroxybenzotriazole (HOBt).

  3. The Organic Chemistry Reaction and Mechanism Guide will help you understand more than 185 of the most common reactions encountered in undergraduate organic chemistry. The guide covers all the necessary reactions from the beginning of Org 1 (Structure and Bonding) to the end of Org 2 (Amino Acids) and everything in-between (Stereochemistry ...

  4. Important Organic Reactions. Important transformations that every synthetic chemist should know are, on the one hand, named reactions in order to be able to discuss them with colleagues, but also frequently used C-C and C-N coupling reactions, since they occur quite often in synthesis plans. Of course, all these Pd-catalyzed cross-coupling ...

  5. Mechanism. TFA (Trifluoroacetic Acid) Examples. Mechanism. TMSI (Trimethylsilyl Iodide) Examples. ZnBr 2 (Zinc Bromide) Examples. A list of common conditions for the boc protection and deprotection of compounds in organic chemistry.

  6. Molecular Weight: 122.17 g/mol. Appearance: White solid. Melting Point: 108-110 C. 4-Dimethylaminopyridine (DMAP) is a nucleophilic catalyst used for numerous different reactions. DMAP is a very effective acyl transfer agent. The use of 4-aminopyridines (such a DMAP) has been shown to speed up the esterification of hindered alcohols via acid ...

  7. Sodium triacetoxyborohydride ( STAB) is a common reducing agent for reductive aminations. STAB is H2O sensitive and not very compatible with MeOH, therefore reactions are typically done in other solvents (ex. DCE, DCM, THF, or dioxane ). Examples. Mechanism.