Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H12O |
| Molecular Weight | 136.191 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C1=CC=C(O)C=C1
InChI
InChIKey=YQUQWHNMBPIWGK-UHFFFAOYSA-N
InChI=1S/C9H12O/c1-7(2)8-3-5-9(10)6-4-8/h3-7,10H,1-2H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Characterization of rabbit UDP-glucuronosyltransferase UGT1A7: tertiary amine glucuronidation is catalyzed by UGT1A7 and UGT1A4. | 1997 Aug 15 |
|
| A lipoxygenase inhibitor from Aspergillus niger. | 2002 Mar |
|
| Genotoxicity evaluation of electromagnetic fields generated by 835-MHz mobile phone frequency band. | 2005 Apr |
|
| Cooperative h-bonds of macromolecules. 1. Binding of low-molecular-weight ligands to polymers. | 2005 Jul 21 |
|
| Biodegradation of phenolic environmental pollutants by a surfactant-laccase complex in organic media. | 2005 Jun |
|
| Bioactivation of bisphenol A and its analogs (BPF, BPAF, BPZ and DMBPA) in human liver microsomes. | 2013 Jun |
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167172
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9F59JOO816
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DTXSID5042299
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99-89-8
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1888
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202-798-8
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7465
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SUBSTANCE RECORD
