Properties and Exciting Facts About 34052-90-9

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 34052-90-9. Application In Synthesis of 1,3-Bis(4,5-dihydrooxazol-2-yl)benzene.

Chemistry, like all the natural sciences, Application In Synthesis of 1,3-Bis(4,5-dihydrooxazol-2-yl)benzene, begins with the direct observation of nature¡ª in this case, of matter.34052-90-9, Name is 1,3-Bis(4,5-dihydrooxazol-2-yl)benzene, SMILES is C1(C2=NCCO2)=CC=CC(C3=NCCO3)=C1, belongs to oxazolidines compound. In a document, author is Singh, Nasseb, introduce the new discover.

A Simple and Efficient Approach for the Synthesis of 1,3-Oxazolidines from beta-Amino Alcohols Using Grinding Technique

An environment-friendly and efficient method for synthesis of 1, 3-oxazolidines from beta-amino alcohols has been developed using paraformaldehyde in the presence of 10 mol% alkali as a green reaction medium. The method is concise, simple, transition metal free, and high yielding at room temperature with wide substrate scope and functional group compatibility. The optimized method can be used for the synthesis of 1, 3-oxazolidines intermediates, which are used as prodrug moieties to improve therapeutic potential of the parent drug. Structure and formation of the synthesized compounds has been characterized and confirmed through conventional spectroscopic techniques, such as H-1 nuclear magnetic resonance (NMR), C-13 NMR, and mass spectroscopy.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 34052-90-9. Application In Synthesis of 1,3-Bis(4,5-dihydrooxazol-2-yl)benzene.

Reference:
Oxazolidine – Wikipedia,
,Oxazolidine | C3H7NO – PubChem