Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H22O2 |
Molecular Weight | 270.3661 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(OOC(C)(C)C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=XMNIXWIUMCBBBL-UHFFFAOYSA-N
InChI=1S/C18H22O2/c1-17(2,15-11-7-5-8-12-15)19-20-18(3,4)16-13-9-6-10-14-16/h5-14H,1-4H3
Approval Year
PubMed
Title | Date | PubMed |
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Role of reactive intermediates in tumor promotion and progression. | 1995 |
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Comparative studies on crosslinked and uncrosslinked natural rubber biodegradation by Pseudomonas sp. | 2006 Dec |
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Lipase-catalyzed synthesis and curing of high-molecular-weight polyricinoleate. | 2007 Jun 7 |
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Gas-phase transfer of polymer cross-linking agents and by-products to solid oral pharmaceuticals. | 2007 Nov 5 |
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A kinetic study of the electron-transfer reaction of the phthalimide-N-oxyl radical (PINO) with ferrocenes. | 2007 Nov 9 |
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Low-molecular-weight model study of peroxide cross-linking of ethylene-propylene (-diene) rubber using gas chromatography and mass spectrometry I. Combination reactions of alkanes. | 2008 Aug 8 |
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Radical scavenging reactivity of catecholamine neurotransmitters and the inhibition effect for DNA cleavage. | 2010 Jan 14 |
Patents
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C037517
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M51X2J0U9D
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80-43-3
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320
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201-279-3
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56772
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DTXSID1025017
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6641
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SUBSTANCE RECORD