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42902-32-9 | 5-(Hydroxymethyl);-3-(4-methoxyphenyl);oxazolidin-2-one
CAS No: 42902-32-9 Catalog No: AG0070TV MDL No:
Product Description
Catalog Number:
AG0070TV
Chemical Name:
5-(Hydroxymethyl);-3-(4-methoxyphenyl);oxazolidin-2-one
CAS Number:
42902-32-9
Molecular Formula:
C11H13NO4
Molecular Weight:
223.2252
IUPAC Name:
5-(hydroxymethyl)-3-(4-methoxyphenyl)-1,3-oxazolidin-2-one
InChI:
InChI=1S/C11H13NO4/c1-15-9-4-2-8(3-5-9)12-6-10(7-13)16-11(12)14/h2-5,10,13H,6-7H2,1H3
InChI Key:
WPBGOVOZPRMHNE-UHFFFAOYSA-N
SMILES:
OCC1CN(C(=O)O1)c1ccc(cc1)OC
Properties
Complexity:
250
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
223.084g/mol
Formal Charge:
0
Heavy Atom Count:
16
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
223.228g/mol
Monoisotopic Mass:
223.084g/mol
Rotatable Bond Count:
3
Topological Polar Surface Area:
59A^2
Undefined Atom Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
XLogP3:
0.8
Literature
| Title | Journal |
|---|---|
| Enantioselective copper-catalysed propargylic substitution: synthetic scope study and application in formal total syntheses of (+)-anisomycin and (-)-cytoxazone. | Chemistry (Weinheim an der Bergstrasse, Germany) 20110516 |
| A strategy to synthesize taxol side chain and (-)-epi cytoxazone via chiral Brønsted acid-Rh(2)(OAc)(4) co-catalyzed enantioselective three-component reactions. | The Journal of organic chemistry 20101105 |
| Co(III)(salen)-catalyzed HKR of two stereocentered alkoxy- and azido epoxides: a concise enantioselective synthesis of (S,S)-reboxetine and (+)-epi-cytoxazone. | Chemical communications (Cambridge, England) 20100721 |
| Highly efficient asymmetric synthesis of vinylic amino alcohols by Zn-promoted benzoyloxyallylation of chiral N-tert-butanesulfinyl imines: facile and rapid access to (-)-cytoxazone. | Chemistry (Weinheim an der Bergstrasse, Germany) 20091005 |
| Regioselective and diastereoselective amination with use of chlorosulfonyl isocyanate: a short and efficient synthesis of (-)-cytoxazone. | Organic letters 20050901 |
| Short-step and scalable synthesis of (+/-)-cytoxazone. | Bioscience, biotechnology, and biochemistry 20050101 |
| Asymmetric synthesis of (4R,5R)-cytoxazone and (4R,5S)-epi-cytoxazone. | Organic & biomolecular chemistry 20040521 |
| A new synthesis of cytoxazone and its diastereomers provides key initial SAR information. | Bioorganic & medicinal chemistry letters 20030407 |
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