Molecule:100617: Difference between revisions
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molecule
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{{Molecule | {{Molecule | ||
|abbrev=PhOH | |||
|trivialname=phenol | |||
|cid=996 | |cid=996 | ||
|iupacName=phenol | |iupacName=phenol | ||
| Line 5: | Line 7: | ||
|molecularFormula=C<sub>6</sub>H<sub>6</sub>O | |molecularFormula=C<sub>6</sub>H<sub>6</sub>O | ||
|logP=1.5 | |logP=1.5 | ||
|synonyms=phenol | |synonyms=phenol$carbolic acid$Hydroxybenzene$Phenic acid$Oxybenzene$Phenylic acid$Phenylic alcohol$Benzenol$Monophenol$Phenyl hydrate | ||
|cas=108-95-2 | |cas=108-95-2 | ||
|hasVendors=true | |hasVendors=true | ||
|moleculeKey=ISWSIDIOOBJBQZ-UHFFFAOYSA-N | |moleculeKey=ISWSIDIOOBJBQZ-UHFFFAOYSA-N | ||
|molOrRxn= | |molOrRxn= | ||
| Line 37: | Line 37: | ||
M V30 END CTAB | M V30 END CTAB | ||
M END | M END | ||
|smiles=C1C=CC=CC=1O | |smiles=C1C=CC=CC=1O | ||
|inchi=1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H | |inchi=1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H | ||
|inchikey=ISWSIDIOOBJBQZ-UHFFFAOYSA-N | |inchikey=ISWSIDIOOBJBQZ-UHFFFAOYSA-N | ||
|width= | |width=150px | ||
|height= | |height=100px | ||
|float=none | |float=none | ||
|parent= | |parent= | ||
}} | }} | ||
Latest revision as of 17:18, 3 May 2024
| Properties | |
|---|---|
| CID | 996 |
| CAS | 108-95-2 |
| IUPAC-Name | phenol |
| Abbreviation | PhOH |
| Trivialname | phenol |
| Exact mass | 94.041864811 |
| Molecular formula | C6H6O |
| LogP | 1.5 |
| Has vendors | true |
| Molecular role | n/a |
| Synonyms | phenol, carbolic acid, Hydroxybenzene, Phenic acid, Oxybenzene, Phenylic acid, Phenylic alcohol, Benzenol, Monophenol, Phenyl hydrate |
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Molecule is used on following pages
topic
publication
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2
- Photocatalytic CO2 Reduction Mediated by Electron Transfer via the Excited Triplet State of Zn(II) Porphyrin
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction
investigation
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Iron-Catalyzed Photochemical CO2 Reduction under diverse conditions
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Iron-Catalyzed Photochemical CO2 Reduction under diverse conditions error
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Table 2 Conversion with Co catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Table 2 conversion with Co catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Table 2 Co catalyst testing
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/testtest2
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Results obtained with Co2+ catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/results CO2+ experiments
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/CO2+ results from SI
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Results Co2+ experiments taken from SI
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/CO2 Reduction under diverse conditions with diverse sensitizers
