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1192-07-0

1192-07-0 | 3-Isoxazolidinone

CAS No: 1192-07-0 Catalog No: AG000IC1 MDL No:MFCD11878032

Product Description

Catalog Number:
AG000IC1
Chemical Name:
3-Isoxazolidinone
CAS Number:
1192-07-0
Molecular Formula:
C3H5NO2
Molecular Weight:
87.0773
MDL Number:
MFCD11878032
IUPAC Name:
1,2-oxazolidin-3-one
InChI:
InChI=1S/C3H5NO2/c5-3-1-2-6-4-3/h1-2H2,(H,4,5)
InChI Key:
QXDOFVVNXBGLKK-UHFFFAOYSA-N
SMILES:
C1CONC1=O

Properties

Complexity:
71.2  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
87.032g/mol
Formal Charge:
0
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
87.078g/mol
Monoisotopic Mass:
87.032g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
38.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.7  

Literature

Title Journal
A diverse series of substituted benzenesulfonamides as aldose reductase inhibitors with antioxidant activity: design, synthesis, and in vitro activity. Journal of medicinal chemistry 20101111
Differential oxidative metabolism and 5-ketoclomazone accumulation are involved in Echinochloa phyllopogon resistance to clomazone. Plant physiology 20100501
Three siderophores from one bacterial enzymatic assembly line. Journal of the American Chemical Society 20090415
Isolation and structure elucidation of parnafungins C and D, isoxazolidinone-containing antifungal natural products. Bioorganic & medicinal chemistry letters 20090215
A latent oxazoline electrophile for N-O-C bond formation in pseudomonine biosynthesis. Journal of the American Chemical Society 20080917
Isolation and structure elucidation of parnafungins, antifungal natural products that inhibit mRNA polyadenylation. Journal of the American Chemical Society 20080604
Synthesis and absolute configuration assignment of 5-amino-1,3,5-triphenyl-pentane-1,3-diol stereoisomers. Chirality 20050101

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