D-glucose as a pentavalent chiral scaffold was written by Opatz, Till;Kallus, Christopher;Wunberg, Tobias;Schmidt, Wolfgang;Henke, Stefan;Kunz, Horst. And the article was included in European Journal of Organic Chemistry in 2003.Safety of 3-Cyanophenylisocyanate This article mentions the following:
A novel carbohydrate-based scaffold for combinatorial chem. has been developed. This scaffold allows the selective attachment of five different side chains, giving rise to products of enormous structural diversity. As a demonstration of its usefulness, a series of model compounds has been prepared in high purity and yield by multistep parallel synthesis on a solid phase. In the experiment, the researchers used many compounds, for example, 3-Cyanophenylisocyanate (cas: 16413-26-6Safety of 3-Cyanophenylisocyanate).
3-Cyanophenylisocyanate (cas: 16413-26-6) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Safety of 3-Cyanophenylisocyanate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics