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209542-84-7 | 2-Oxazolidinone, 3-[(2Z)-1-oxo-2-buten-1-yl]-
CAS No: 209542-84-7 Catalog No: AG002KAK MDL No:
Product Description
Catalog Number:
AG002KAK
Chemical Name:
2-Oxazolidinone, 3-[(2Z)-1-oxo-2-buten-1-yl]-
CAS Number:
209542-84-7
Molecular Formula:
C7H9NO3
Molecular Weight:
155.1513
IUPAC Name:
3-but-2-enoyl-1,3-oxazolidin-2-one
InChI:
InChI=1S/C7H9NO3/c1-2-3-6(9)8-4-5-11-7(8)10/h2-3H,4-5H2,1H3
InChI Key:
PNPVETUIPHVXGI-UHFFFAOYSA-N
SMILES:
C/C=C\C(=O)N1CCOC1=O
Properties
Complexity:
210
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
155.058g/mol
Formal Charge:
0
Heavy Atom Count:
11
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
155.153g/mol
Monoisotopic Mass:
155.058g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
46.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
1
XLogP3:
0.5
Literature
| Title | Journal |
|---|---|
| Highly enantioselective conjugate addition of thiols using mild scandium triflate catalysis. | The Journal of organic chemistry 20070706 |
| The remarkable ability of lithium ion to reverse the stereoselectivity in the conjugate addition of Li[BuCuI] to a chiral N-crotonyl-2-oxazolidinone. | Organic letters 20030918 |
| Preparation and characterization of TADDOLs immobilized on hydrophobic controlled-pore-glass silica gel and their use in enantioselective heterogeneous catalysis. | Chemistry (Weinheim an der Bergstrasse, Germany) 20020202 |
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