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15596-07-3 | Ethenone, 2-(triphenylphosphoranylidene)-
CAS No: 15596-07-3 Catalog No: AG001ODY MDL No:MFCD00040613
Product Description
Catalog Number:
AG001ODY
Chemical Name:
Ethenone, 2-(triphenylphosphoranylidene)-
CAS Number:
15596-07-3
Molecular Formula:
C20H15OP
Molecular Weight:
302.3063
MDL Number:
MFCD00040613
IUPAC Name:
2-(triphenyl-λ5-phosphanylidene)ethenone
InChI:
InChI=1S/C20H15OP/c21-16-17-22(18-10-4-1-5-11-18,19-12-6-2-7-13-19)20-14-8-3-9-15-20/h1-15H
InChI Key:
MNASRBWCHRURHY-UHFFFAOYSA-N
SMILES:
O=C=C=P(c1ccccc1)(c1ccccc1)c1ccccc1
NSC Number:
620573
Properties
Complexity:
400
Compound Is Canonicalized:
No
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
302.086g/mol
Formal Charge:
0
Heavy Atom Count:
22
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
302.313g/mol
Monoisotopic Mass:
302.086g/mol
Rotatable Bond Count:
3
Topological Polar Surface Area:
17.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.5
Literature
| Title | Journal |
|---|---|
| Anhydrous TEMPO-H: reactions of a good hydrogen atom donor with low-valent carbon centres. | Organic & biomolecular chemistry 20110521 |
| Tetramic and tetronic acids as scaffolds in bioinorganic and bioorganic chemistry. | Bioinorganic chemistry and applications 20100101 |
| Facile preparation and functionalization of chiral stabilized ylides from common chiral auxiliaries using triphenyl- phosphoranylideneketene (the Bestmann ylide) and their use in Wittig reactions. | The Journal of organic chemistry 20061110 |
| Cascade synthesis with (triphenylphosphoranylidene)-ethenone as a versatile reagent for fast synthesis of heterocycles and unsaturated amides under microwave dielectric heating. | Combinatorial chemistry & high throughput screening 20021101 |
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