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504-76-7 | 1,3-Oxazolidine
CAS No: 504-76-7 Catalog No: AG00DJGL MDL No:MFCD16251479
Product Description
Catalog Number:
AG00DJGL
Chemical Name:
1,3-Oxazolidine
CAS Number:
504-76-7
Molecular Formula:
C3H7NO
Molecular Weight:
73.0938
MDL Number:
MFCD16251479
IUPAC Name:
1,3-oxazolidine
InChI:
InChI=1S/C3H7NO/c1-2-5-3-4-1/h4H,1-3H2
InChI Key:
WYNCHZVNFNFDNH-UHFFFAOYSA-N
SMILES:
C1NCCO1
EC Number:
610-533-6
UNII:
13F52UF6MR
Properties
Complexity:
30.1
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
73.053g/mol
Formal Charge:
0
Heavy Atom Count:
5
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
73.095g/mol
Monoisotopic Mass:
73.053g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
21.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.5
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| Synthesis and structure-activity relationships of open D-Ring galanthamine analogues. | Bioorganic & medicinal chemistry letters 20030721 |
| Tandem formation and [2,3] rearrangement of methylene ammonium ylides derived from amines and the Simmons-Smith reagent. | Organic letters 20030515 |
| Inhibition of the D-fructose transporter protein GLUT5 by fused-ring glyco-1,3-oxazolidin-2-thiones and -oxazolidin-2-ones. | Carbohydrate research 20030404 |
| Mechanism of human S-adenosylmethionine decarboxylase proenzyme processing as revealed by the structure of the S68A mutant. | Biochemistry 20030304 |
| First asymmetric synthesis of 6-hydroxy-4-sphingenine-containing ceramides. Use of chiral propargylic alcohols to prepare a lipid found in human skin. | The Journal of organic chemistry 20030124 |
| Mass spectral fragmentation of (S,S)-2-substituted 4,4-diphenyl-3,1-oxazabicyclo[3.3.0]octanes: ring contraction of pyrrolidine and 1,3-oxazolidine in mass spectrometry. | Rapid communications in mass spectrometry : RCM 20030101 |
| Electrospray mass spectrometry determination of poly(oxazolidine acetal). | Rapid communications in mass spectrometry : RCM 20030101 |
| Inhibitors of calling behavior of Plodia interpunctella. | Journal of insect science (Online) 20030101 |
| Three-dimensional common-feature hypotheses of inhibitors of calling behaviour and in vitro [14C]acetate incorporation by pheromone glands of Plodia interpunctella. | Pest management science 20021101 |
| Mutagenic effects of cutting fluids and components in the Salmonella typhimurium mutagenicity assay. | Toxicology and industrial health 20021001 |
| Synthesis of a polymer-supported oxazolidine aldehyde for asymmetric chemistry. | The Journal of organic chemistry 20020920 |
| Antiplatelet aggregation activity of diterpene alkaloids from Spiraea japonica. | European journal of pharmacology 20020802 |
| Asymmetric synthesis of a selective endothelin A receptor antagonist. | Chemical & pharmaceutical bulletin 20020801 |
| Ring-opening reactions of cyclic acetals and 1,3-oxazolidines with halosilane equivalents. | The Journal of organic chemistry 20020726 |
| Synthesis of alpha- and beta-glycosyl asparagine ethylene isosteres (C-glycosyl asparagines) via sugar acetylenes and Garner aldehyde coupling. | The Journal of organic chemistry 20020628 |
| Practical and highly selective oxazolidinethione-based asymmetric acetate aldol reactions with aliphatic aldehydes. | Organic letters 20020627 |
| Synthesis of new trans double-bond sphingolipid analogues: Delta(4,6) and Delta(6) ceramides. | The Journal of organic chemistry 20020419 |
| Enantioselective synthesis of N(alpha)-Fmoc protected (2S,3R)-3-phenylpipecolic acid. A constrained phenylalanine analogue suitably protected for solid-phase peptide synthesis. | The Journal of organic chemistry 20020308 |
| Modified guanines representing O(6)-alkylation by the cyclophosphamide metabolites acrolein and chloroacetaldehyde: synthesis, stability, and ab initio studies. | Chemical research in toxicology 20020301 |
| Intermethod comparisons of active sampling procedures and analysis of aldehydes at environmental levels. | Analytical and bioanalytical chemistry 20020301 |
| A new method for the synthesis of ranitidine. | Acta poloniae pharmaceutica 20020101 |
| Carbinolamines, imines, and oxazolidines from fluorinated propranolol analogs. (19)F NMR and mass spectral characterization and evidence for formation as intermediates in cytochrome P450-catalyzed N-dealkylation. | Drug metabolism and disposition: the biological fate of chemicals 20010801 |
| Access to the inaccessible sequence of cpn 60.1 (195-217) by temporary oxazolidine protection of selected amide bonds. | Bioorganic & medicinal chemistry letters 20010326 |
| Diastereoselective epoxidation of oxazolidine-substituted alkenes by dimethyldioxirane and m-chloroperbenzoic acid: pi-facial control through hydrogen bonding by the urea functionality. | Organic letters 20010111 |
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