Some scientific research about (S)-4-Phenyloxazolidin-2-one

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 99395-88-7. Recommanded Product: (S)-4-Phenyloxazolidin-2-one.

Chemistry, like all the natural sciences, begins with the direct observation of nature¡ª in this case, of matter.99395-88-7, Name is (S)-4-Phenyloxazolidin-2-one, SMILES is [C@H]1(NC(OC1)=O)C2=CC=CC=C2, belongs to oxazolidines compound. In a document, author is Inada, Aya, introduce the new discover, Recommanded Product: (S)-4-Phenyloxazolidin-2-one.

Crystal structure of O-benzyl-L-tyrosine-N-carboxy anhydride

In the title compound, C17H15NO4 {alternative name: (S)-4-[4-(benzyloxy)benzyl]oxazolidine-2,5-dione}, the oxazolidine ring is planer, with an r.m.s. deviation of 0.039 angstrom. The benzyloxy and benzyl rings are almost coplanar, making a dihedral angle of 0.078 (10)degrees, and are inclined to the oxazolidine ring by 59.16 (11) and 58.42 (11)degrees, respectively. In the crystal, molecules are linked by N-H center dot center dot center dot O and C-H center dot center dot center dot O hydrogen bonds, forming ribbons propagating along [010]. The ribbons are linked by C-H center dot center dot center dot pi interactions, forming a threedimensional supramolecular structure. The oxazolidine rings of adjacent ribbons are arranged into a layer parallel to the ab plane. This arrangement is favourable for the polymerization of the compound in the solid state.

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 99395-88-7. Recommanded Product: (S)-4-Phenyloxazolidin-2-one.

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