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6542-34-3 | 2-Oxazolin-4-one
CAS No: 6542-34-3 Catalog No: AG00F40V MDL No:
Product Description
Catalog Number:
AG00F40V
Chemical Name:
2-Oxazolin-4-one
CAS Number:
6542-34-3
IUPAC Name:
1,3-oxazol-4-one
InChI:
InChI=1S/C3H3NO2/c5-3-1-6-2-4-3/h2H,1H2
InChI Key:
KCOPAESEGCGTKM-UHFFFAOYSA-N
Properties
Complexity:
97
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
85.016g/mol
Formal Charge:
0
Heavy Atom Count:
6
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
85.062g/mol
Monoisotopic Mass:
85.016g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
38.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.2
Literature
| Title | Journal |
|---|---|
| In vitro reconstitution of indolmycin biosynthesis reveals the molecular basis of oxazolinone assembly. | Proceedings of the National Academy of Sciences of the United States of America 20150303 |
| Palladium-catalyzed allylic alkylation of carboxylic acid derivatives: N-acyloxazolinones as ester enolate equivalents. | Angewandte Chemie (International ed. in English) 20120102 |
| Poly(3-alkylthiophenes): new sorption materials for solid phase microextraction of drugs isolated from human plasma. | Analytical and bioanalytical chemistry 20110901 |
| Nickel/bis(oxazoline)-catalyzed asymmetric Kumada reactions of alkyl electrophiles: cross-couplings of racemic alpha-bromoketones. | Journal of the American Chemical Society 20100203 |
| Introducing N-glycans into natural products through a chemoenzymatic approach. | Carbohydrate research 20081124 |
| Synthetic approaches to N(delta)-methylated L-arginine, N(omega)-hydroxy-L-arginine, L-citrulline, and N(delta)-cyano-L-ornithine. | The Journal of organic chemistry 20080201 |
| N-tosyloxycarbamates as reagents in rhodium-catalyzed C-H amination reactions. | Chemistry (Weinheim an der Bergstrasse, Germany) 20080101 |
| Aldol reactions between L-erythrulose derivatives and chiral alpha-amino and alpha-fluoro aldehydes: competition between Felkin-Anh and Cornforth transition states. | Chemistry (Weinheim an der Bergstrasse, Germany) 20080101 |
| Toward iron sensors: bioinspired tripods based on fluorescent phenol-oxazoline coordination sites. | Inorganic chemistry 20070402 |
| Stereoselective synthesis of benzomorphan derivatives with perpivaloylated galactose as the chiral auxiliary. | Angewandte Chemie (International ed. in English) 20060410 |
| Synthesis and biological evaluation of simplified mycothiazole analogues. | Bioorganic & medicinal chemistry letters 20060301 |
| Highly efficient endoglycosidase-catalyzed synthesis of glycopeptides using oligosaccharide oxazolines as donor substrates. | Journal of the American Chemical Society 20050713 |
| Enantioselective synthesis of six-membered palladacycles having metal-bound stereogenic carbons: isolation and reactivity of palladacycles containing readily accessible beta-hydrogens. | Journal of the American Chemical Society 20041229 |
| Ciprofloxacin-induced acute psychosis in a patient with multidrug-resistant tuberculosis. | European psychiatry : the journal of the Association of European Psychiatrists 20030801 |
| High-throughput catch-and-release synthesis of oxazoline hydroxamates. Structure-activity relationships in novel inhibitors of Escherichia coli LpxC: in vitro enzyme inhibition and antibacterial properties. | Journal of the American Chemical Society 20030212 |
| Polymer-supported ferrocenyl oxazolines for the catalyzed highly enantioselective phenyl transfer to aldehydes. | Bioorganic & medicinal chemistry letters 20020722 |
| Oxazolinone derivative of leucine for GC-MS: a sensitive and robust method for stable isotope kinetic studies of lipoproteins. | Journal of lipid research 20020201 |
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