Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H5O.K |
| Molecular Weight | 132.2016 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[K+].[O-]C1=CC=CC=C1
InChI
InChIKey=ZGJADVGJIVEEGF-UHFFFAOYSA-M
InChI=1S/C6H6O.K/c7-6-4-2-1-3-5-6;/h1-5,7H;/q;+1/p-1
PubMed
| Title | Date | PubMed |
|---|---|---|
| Effects of charge separation, effective concentration, and aggregate formation on the phase transfer catalyzed alkylation of phenol. | 2012-08-15 |
|
| Synthesis of indole-3-carboxylic acid derivatives by Pd(0)-catalyzed intramolecular alpha-arylation of beta-(2-iodoanilino) esters. | 2008-03-21 |
|
| Mechanism of the Kolbe-Schmitt reaction. Structure of the intermediate potassium phenoxide-CO(2) complex. | 2007-05-22 |
|
| Synthesis of the 4-azatricyclo[5.2.2.0(4,8)]undecan-10-one core of daphniphyllum alkaloid calyciphylline A using a Pd-catalyzed enolate alkenylation. | 2005-11-24 |
Patents
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DTXSID30881405
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9CQ00ODF3U
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202-877-7
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23670670
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m9048
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100-67-4
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PARENT (SALT/SOLVATE)
SUBSTANCE RECORD
