A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 21436-03-3, Name is (1S,2S)-Cyclohexane-1,2-diamine, molecular formula is C6H14N2. In a Review，once mentioned of 21436-03-3, Safety of (1S,2S)-Cyclohexane-1,2-diamine
The unique structure of BINOL has been extensively used for enantioselective molecular recognition, which can be monitored by many detecting means, such as fluorescence, UVevis absorption, CD, electrochemistry, HPLC, NMR and X-ray crystallography. Various types of functional groups have been attached to the enantiomerically pure BINOL to build small molecules, dendrimers, oligomers, polymers, MOFs, HOFs and CSPs. These chiral materials not only differentiate two enantiomers of chiral substrates, but also have achieved rapid determination of ee, separation of racemic samples and chirality conversion for organic compounds including chiral amines, alcohols, carboxylic acids, ketones and sulfoxides. The research on the BINOL-based molecules has great potentials for many practical applications such as rapid chiral assay and chiral resolution. Thus, one would expect the continuous development of the BINOL chemistry in many research areas.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Safety of (1S,2S)-Cyclohexane-1,2-diamine. In my other articles, you can also check out more blogs about 21436-03-3