2,3-Dihydro-1H-inden-1-ol
2,3-Dihydro-1H-inden-1-ol structure
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Common Name | 2,3-Dihydro-1H-inden-1-ol | ||
|---|---|---|---|---|
| CAS Number | 6351-10-6 | Molecular Weight | 134.175 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 255.1±9.0 °C at 760 mmHg | |
| Molecular Formula | C9H10O | Melting Point | 50-53 °C | |
| MSDS | Chinese USA | Flash Point | 89.2±11.0 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Naturally occurring variants of human aldo-keto reductases with reduced in vitro metabolism of daunorubicin and doxorubicin.
J. Pharmacol. Exp. Ther. 335 , 533-545, (2010) Doxorubicin (DOX) and daunorubicin (DAUN) are effective anticancer drugs; however, considerable interpatient variability exists in their pharmacokinetics. This may be caused by altered metabolism by nonsynonymous single-nucleotide polymorphisms (ns-SNPs) in g... |
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Determination of the single component and competitive adsorption isotherms of the 1-indanol enantiomers by the inverse method.
J. Chromatogr. A. 1005(1-2) , 35-49, (2003) The inverse method of isotherm determination consists in calculating the numerical values of the coefficients of an isotherm model that give a set of chromatographic profiles in best possible agreement with the set of experimental profiles available. This met... |
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Conformational landscapes and free-jet rotational spectrum of indan-1-ol.
ChemPhysChem 7(3) , 565-8, (2006)
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Desaturation, dioxygenation, and monooxygenation reactions catalyzed by naphthalene dioxygenase from Pseudomonas sp. strain 9816-4.
J. Bacteriol. 177(10) , 2615-21, (1995) The stereospecific oxidation of indan and indene was examined with mutant and recombinant strains expressing naphthalene dioxygenase of Pseudomonas sp. strain 9816-4. Pseudomonas sp. strain 9816/11 and Escherichia coli JM109(DE3)[pDTG141] oxidized indan to (+... |
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Heterogeneous adsorption of 1-indanol on cellulose tribenzoate and adsorption energy distribution of the two enantiomers.
Anal. Chem. 76(1) , 197-202, (2004) The distributions of the adsorption energies (AED) of two enantiomers, (R)-1- indanol and (S)-1-indanol, on a chiral stationary phase were measured and the results are discussed. The chiral phase used is made of cellulose tribenzoate coated on porous silica. ... |
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Stereospecific oxidation of (R)- and (S)-1-indanol by naphthalene dioxygenase from Pseudomonas sp. strain NCIB 9816-4.
Appl. Environ. Microbiol. 63(5) , 2067-70, (1997) A recombinant Escherichia coli strain which expresses naphthalene dioxygenase (NDO) from Pseudomonas sp. strain NCIB 9816-4 oxidized (S)-1-indanol to trans-(1S,3S)-indan-1,3-diol (95.5%) and (R)-3-hydroxy-1-indanone (4.5%). The same cells oxidized (R)-1-indan... |
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Development of a bioconversion process for production of cis-1S,2R-indandiol from indene by recombinant Escherichia coli constructs.
Appl. Microbiol. Biotechnol. 51(5) , 614-20, (1999) Recombinant Escherichia coli cells expressing the toluene dioxygenase (TDO) genes from Pseudomonas putida convert indene to cis-1S,2R-indandiol, a potentially important intermediate for the chemical synthesis of the HIV-1 protease inhibitor, Crixivan. A bioco... |
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Comparison of the binary equilibrium isotherms of the 1-indanol enantiomers on three high-performance liquid chromatography columns of different sizes.
J. Chromatogr. A. 1015(1-2) , 73-87, (2003) The competitive isotherm data for the enantiomers of 1-indanol were measured on three columns, a microbore column (15 cm x 0.1 cm), a conventional analytical column (15 cm x 0.46 cm), and a semi-preparative column (20 cm x 1.0 cm), packed with Chiralcel OB. T... |
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Kinetic studies of the inhibition of a human liver 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase isozyme by bile acids and anti-inflammatory drugs.
Biol. Pharm. Bull. 18(1) , 9-12, (1995) We have investigated the steady-state kinetics for a cytosolic 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase isozyme of human liver and its inhibition by several bile acids and anti-inflammatory drugs such as indomethacin, flufemanic acid and naproxen. Ini... |
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Chirality-dependent balance between hydrogen bonding and London dispersion in isolated (±)-1-indanol clusters.
Phys. Chem. Chem. Phys. 15(25) , 10167-80, (2013) The aggregation behavior of racemic and enantiopure 1-indanol has been studied by FTIR spectroscopy, resonant ion dip IR spectroscopy, and spontaneous Raman scattering in supersonic jets. This triple experimental approach, augmented by homology to related mol... |