Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C9H12O |
| Molecular Weight | 136.191 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(O)CC1=CC=CC=C1
InChI
InChIKey=WYTRYIUQUDTGSX-UHFFFAOYSA-N
InChI=1S/C9H12O/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8,10H,7H2,1H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| S-Substituted cysteine derivatives and thiosulfinate formation in Petiveria alliacea-part II. | 2002 Nov |
|
| Microbial degradation of illicit drugs, their precursors, and manufacturing by-products: implications for clandestine drug laboratory investigation and environmental assessment. | 2003 Jun 24 |
|
| Rotational spectra and conformational structures of 1-phenyl-2-propanol, methamphetamine, and 1-phenyl-2-propanone. | 2006 Dec 14 |
|
| Enantioseparation of secondary alcohols by diastereoisomeric salt formation. | 2006 Feb |
|
| Effect of sample solvent on the chromatographic peak shape of analytes eluted under reversed-phase liquid chromatogaphic conditions. | 2006 Jun 30 |
|
| Purification and characterization of alcohol dehydrogenase reducing N-benzyl-3-pyrrolidinone from Geotrichum capitatum. | 2007 Feb |
|
| A Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase mutant derivative highly active and stereoselective on phenylacetone and benzylacetone. | 2007 Feb |
|
| The FEMA GRAS assessment of aromatic substituted secondary alcohols, ketones, and related esters used as flavor ingredients. | 2007 Feb |
|
| Improved synthesis of (S)-1-phenyl-2-propanol in high concentration with coupled whole cells of Rhodococcus erythropolis and Bacillus subtilis on preparative scale. | 2010 Nov |
Patents
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| Code System | Code | Type | Description | ||
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53553
Created by
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1180015
Created by
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DTXSID70862379
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300Y7TB8EY
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211-821-0
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698-87-3
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94185
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SUBSTANCE RECORD
