2,5-Oxazolidinedione, 4-(1-methylethyl)-, (S)-


Chemical Name: 2,5-Oxazolidinedione, 4-(1-methylethyl)-, (S)-
CAS Number: 24601-74-9
Product Number: AG002OPE(AGN-PC-0O87BZ)
Synonyms:
MDL No:
Molecular Formula: C6H9NO3
Molecular Weight: 143.1406

Identification/Properties


Properties
MP:
70-71°C
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
143.142g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
143.058g/mol
Monoisotopic Mass:
143.058g/mol
Topological Polar Surface Area:
55.4A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
176
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



(S)-4-Isopropyloxazolidine-2,5-dione is a versatile compound widely employed in chemical synthesis for its unique properties and reactivity. This chiral oxazolidine derivative serves as an important building block in various organic transformations, particularly in asymmetric synthesis and medicinal chemistry. Its asymmetric nature and functional groups make it a valuable reagent for the synthesis of enantiomerically pure compounds with high optical purity. The (S)-4-Isopropyloxazolidine-2,5-dione can act as a chiral auxiliary, enabling the asymmetric induction in reactions, leading to the formation of stereochemically enriched molecules. Additionally, this compound is utilized in the preparation of pharmaceutical intermediates, agrochemicals, and fine chemicals where stereocontrol is crucial for the biological activity or desired properties of the target molecules. Its efficient use in chemical synthesis has made it a valuable tool in the hands of synthetic chemists for the construction of complex molecular architectures with precise stereochemistry.