191090-34-3 Usage
Description
(S)-(-)-5,5-DIPHENYL-4-ISOBUTYL-2-OXAZOLIDINONE is a chiral chemical compound belonging to the oxazolidinone family. It is characterized by its unique structure, which includes a five-membered ring containing an oxygen and nitrogen atom, with phenyl and isobutyl substituents attached. The (S)-(-) designation represents the stereochemistry of the molecule, indicating that it has a non-superimposable mirror image. (S)-(-)-5,5-DIPHENYL-4-ISOBUTYL-2-OXAZOLIDINONE is widely recognized for its use as a chiral auxiliary in asymmetric synthesis, where it helps control the stereochemistry of chemical reactions. Furthermore, it has shown biological activities and is currently under investigation for potential pharmaceutical applications.
Uses
Used in Pharmaceutical Applications:
(S)-(-)-5,5-DIPHENYL-4-ISOBUTYL-2-OXAZOLIDINONE is used as a chiral auxiliary in the pharmaceutical industry for controlling the stereochemistry of chemical reactions. Its unique structure and stereochemistry enable the synthesis of complex molecules with specific configurations, which are crucial for the development of effective and selective drugs.
Used in Asymmetric Synthesis:
In the field of organic chemistry, (S)-(-)-5,5-DIPHENYL-4-ISOBUTYL-2-OXAZOLIDINONE is employed as a chiral auxiliary for asymmetric synthesis. It plays a vital role in controlling the stereochemistry of chemical reactions, leading to the formation of enantiomerically pure compounds. This is particularly important in the synthesis of biologically active molecules, as the stereochemistry of a molecule can significantly influence its biological activity and selectivity.
Used in Research and Development:
(S)-(-)-5,5-DIPHENYL-4-ISOBUTYL-2-OXAZOLIDINONE is also utilized in research and development for the exploration of its potential pharmaceutical applications. Its biological activities and unique structural features make it an interesting candidate for the development of new drugs and therapeutic agents. Researchers are actively investigating its properties and potential uses in various therapeutic areas, including but not limited to, the treatment of various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 191090-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,0,9 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 191090-34:
(8*1)+(7*9)+(6*1)+(5*0)+(4*9)+(3*0)+(2*3)+(1*4)=123
123 % 10 = 3
So 191090-34-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H21NO2/c1-14(2)13-17-19(22-18(21)20-17,15-9-5-3-6-10-15)16-11-7-4-8-12-16/h3-12,14,17H,13H2,1-2H3,(H,20,21)/t17-/m0/s1
191090-34-3Relevant articles and documents
A short synthesis of (S)-α-(diphenylmethyl)alkyl amines from amino acids
O'Hagan, David,Tavasli, Mustafa
, p. 1189 - 1192 (2007/10/03)
A range of (S)-α-(diphenylmethyl)alkyl amines were prepared from the corresponding (S)-α-amino acid ester hydrochlorides. These amines were derived by direct hydrogenation of their precursor oxazolidinones.
