3-Oxatricyclo[4.1.1.02,4]octane,2,7,7-trimethyl-
![3-Oxatricyclo[4.1.1.02,4]octane,2,7,7-trimethyl- Structure](https://image.chemsrc.com/caspic/466/1686-14-2.png)
3-Oxatricyclo[4.1.1.02,4]octane,2,7,7-trimethyl- structure
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Common Name | 3-Oxatricyclo[4.1.1.02,4]octane,2,7,7-trimethyl- | ||
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| CAS Number | 1686-14-2 | Molecular Weight | 152.23300 | |
| Density | 1.027g/cm3 | Boiling Point | 102 - 103ºC at 30 mm Hg | |
| Molecular Formula | C10H16O | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 65.6ºC | |
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Secondary organic aerosol from alpha-pinene ozonolysis in dynamic chamber system.
Indoor Air 19(4) , 335-45, (2009) The formation of secondary organic aerosol (SOA) produced from alpha-pinene ozonolysis was examined using a dynamic chamber system that allowed the simulation of ventilated indoor environments. Particle-bound reactive species (ROS) including peroxides, peroxy... |
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Improvement of P450(BM-3) whole-cell biocatalysis by integrating heterologous cofactor regeneration combining glucose facilitator and dehydrogenase in E. coli.
Appl. Microbiol. Biotechnol. 78(1) , 55-65, (2008) Escherichia coli BL21, expressing a quintuple mutant of P450(BM-3), oxyfunctionalizes alpha-pinene in an NADPH-dependent reaction to alpha-pinene oxide, verbenol, and myrtenol. We optimized the whole-cell biocatalyst by integrating a recombinant intracellular... |
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Optimization of isonovalal production from alpha-pinene oxide using permeabilized cells of Pseudomonas rhodesiae CIP 107491.
Appl. Microbiol. Biotechnol. 60(5) , 534-40, (2003) Optimization studies on the synthesis of isonovalal from alpha-pinene oxide by Pseudomonas rhodesiae CIP 107491 operated in a biphasic medium are presented. Three key parameters are identified. The first is the need for a permeabilization of cells by freezing... |
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Discovery of synergistic permeation enhancers for oral drug delivery.
J. Control. Release 128(2) , 128-33, (2008) Oral drug delivery offers an attractive method of needle-free drug administration. Unfortunately, oral delivery is often hampered by the poor permeability of drugs across the intestinal epithelium. Although several single chemical permeation enhancers have be... |
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Bacterial metabolism of alpha-pinene: pathway from alpha-pinene oxide to acyclic metabolites in Nocardia sp. strain P18.3.
J. Bacteriol. 169(11) , 4972-9, (1987) Over 20 gram-positive bacteria were isolated by elective culture with (+/-)-alpha-pinene as the sole carbon source. One of these strains, Nocardia sp. strain P18.3, was selected for detailed study. alpha-Pinene-grown cells oxidized, without lag, alpha-pinene,... |
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Production of trans-2-methyl-5-isopropylhexa-2,5-dienoic acid by Pseudomonas rhodesiae CIP 107491.
Bioresour. Technol. 99(11) , 4590-6, (2008) The feasibility of trans-2-methyl-5-isopropylhexa-2,5-dienoic acid (novalic acid) accumulation using the alpha-pinene degradation pathway of Pseudomonas rhodesiae CIP 107491 was studied. This appeared possible by using concentrated living bacterial cells prod... |
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A membrane bioreactor for the biotransformation of alpha-pinene oxide to isonovalal by Pseudomonas fluorescens NCIMB 11671.
Appl. Microbiol. Biotechnol. 69(6) , 643-9, (2006) In this work the biotransformation of alpha-pinene oxide to isonovalal using resting cells of Pseudomonas fluorescens NCIMB 11671 was evaluated in a membrane bioreactor for biotransformations (MBB). Since the membrane area required to obtain optimum productiv... |
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Series: 'Current issues in mutagenesis and carcinogenesis', No. 25.
Mutat. Res. 260(1) , 5-7, (1991)
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Mass spectrometric studies of DNA adducts from a reaction with terpenoids.
Angew. Chem. Int. Ed. Engl. 43(48) , 6657-60, (2004)
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Degradation of alpha-pinene oxide and [2H7]-2,5,6-trimethyl-hept-(2E)-enoic acid by Pseudomonas fluorescens NCIMB 11761.
J. Biotechnol. 107(3) , 255-63, (2004) When submerged cultured Pseudomonas fluorescens NCIMB 11761 was fed-batch supplemented with alpha-pinene oxide, a rapid formation of 2,6-dimethyl-5-methylene-hept-(2Z)-enal (I) (isonovalal) was observed. Biotransformation and isomerisation of (I) to the (2E)-... |