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778-66-5 | Prop-1-ene-1,1-diyldibenzene
CAS No: 778-66-5 Catalog No: AG0036MX MDL No:MFCD00136991
Product Description
Catalog Number:
AG0036MX
Chemical Name:
Prop-1-ene-1,1-diyldibenzene
CAS Number:
778-66-5
Molecular Formula:
C15H14
Molecular Weight:
194.2717
MDL Number:
MFCD00136991
IUPAC Name:
1-phenylprop-1-enylbenzene
InChI:
InChI=1S/C15H14/c1-2-15(13-9-5-3-6-10-13)14-11-7-4-8-12-14/h2-12H,1H3
InChI Key:
KYVBUUNCHXRYOS-UHFFFAOYSA-N
SMILES:
CC=C(c1ccccc1)c1ccccc1
NSC Number:
42487
Properties
Complexity:
182
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
194.11g/mol
Formal Charge:
0
Heavy Atom Count:
15
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
194.277g/mol
Monoisotopic Mass:
194.11g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.8
Literature
| Title | Journal |
|---|---|
| Competitive enantiodifferentiating anti-Markovnikov photoaddition of water and methanol to 1,1-diphenylpropene using a sensitizing cyclodextrin host. | The Journal of organic chemistry 20090904 |
| Supramolecular complexation and photochirogenesis with inherently chiral molecular clip: enantiodifferentiating photoisomerization of (Z,Z)-1,3-cyclooctadiene and polar photoaddition to 1,1-diphenylpropene. | Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20081201 |
| Sequential and selective hydrogenation of the C(alpha)-C(beta) and M-C(alpha) double bonds of an allenylidene ligand coordinated to osmium: new reaction patterns between an allenylidene complex and alcohols. | Journal of the American Chemical Society 20070718 |
| The first supramolecular photosensitization of enantiodifferentiating bimolecular reaction: anti-Markovnikov photoaddition of methanol to 1,1-diphenylpropene sensitized by modified beta-cyclodextrin. | Chemical communications (Cambridge, England) 20060428 |
| A superior P-H phosphonite: asymmetric allylic substitutions with fenchol-based palladium catalysts. | Beilstein journal of organic chemistry 20060101 |
| Enantiodifferentiating photoaddition of alcohols to 1,1-diphenylpropene in supercritical carbon dioxide: sudden jump of optical yield at the critical density. | Journal of the American Chemical Society 20040602 |
| Pressure control of enantiodifferentiating polar addition of 1,1-diphenylpropene sensitized by chiral naphthalenecarboxylates. | Organic & biomolecular chemistry 20040507 |
| Microenvironmental polarity control of electron-transfer photochirogenesis. Enantiodifferentiating polar addition of 1,1-diphenyl-1-alkenes photosensitized by saccharide naphthalenecarboxylates. | Journal of the American Chemical Society 20030312 |
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