Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H14O |
| Molecular Weight | 150.2176 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(O)CCC1=CC=CC=C1
InChI
InChIKey=GDWRKZLROIFUML-UHFFFAOYSA-N
InChI=1S/C10H14O/c1-9(11)7-8-10-5-3-2-4-6-10/h2-6,9,11H,7-8H2,1H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Nonaqueous and halide-free route to crystalline BaTiO3, SrTiO3, and (Ba,Sr)TiO3 nanoparticles via a mechanism involving C-C bond formation. | 2004 Jul 28 |
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| Aminocyclopentadienyl ruthenium complexes as racemization catalysts for dynamic kinetic resolution of secondary alcohols at ambient temperature. | 2004 Mar 19 |
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| A Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase mutant derivative highly active and stereoselective on phenylacetone and benzylacetone. | 2007 Feb |
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| Use of perfluorinated phosphines to provide thermomorphic anticancer complexes for heat-based tumor targeting. | 2010 Mar 1 |
|
| Aminodifluorosulfinium salts: selective fluorination reagents with enhanced thermal stability and ease of handling. | 2010 May 21 |
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CFR |
21 CFR 172.515
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JECFA EVALUATION |
4-PHENYL-2-BUTANOL
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admin on Fri Dec 15 17:53:46 GMT 2023 , Edited by admin on Fri Dec 15 17:53:46 GMT 2023
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SZ2IE5UDQR
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2344-70-9
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69076
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61302
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DTXSID60862904
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219-055-9
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803
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SUBSTANCE RECORD
