Cyclopentanol
Cyclopentanol structure
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Common Name | Cyclopentanol | ||
|---|---|---|---|---|
| CAS Number | 96-41-3 | Molecular Weight | 86.132 | |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 140.8±0.0 °C at 760 mmHg | |
| Molecular Formula | C5H10O | Melting Point | -19 °C | |
| MSDS | Chinese USA | Flash Point | 51.1±0.0 °C | |
| Symbol |
GHS02 |
Signal Word | Warning | |
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Convenient QSAR model for predicting the complexation of structurally diverse compounds with β-cyclodextrins
Bioorg. Med. Chem. 17 , 896-904, (2009) This paper reports a QSAR study for predicting the complexation of a large and heterogeneous variety of substances (233 organic compounds) with beta-cyclodextrins (beta-CDs). Several different theoretical molecular descriptors, calculated solely from the mole... |
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Optical, Electrochemical and Thermoanalytical Investigations on Newly-Synthesized Perylene-3,4,9,10-Dianhydride Fluorescent Dyes.
J. Fluoresc. 25 , 1045-53, (2015) A series of dyes using tetrachloroperylene dianhydride as fluorescent chromophore was synthesized by the substitution of suitable aliphatic and alicyclic alcohols in alkaline medium, and evaluation of dyes was done for their optical, electrochemical and therm... |
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New enzymatic assay for the AKR1C enzymes.
Chem. Biol. Interact. 202(1-3) , 204-9, (2013) The imbalance in expression of the human aldo-keto reductases AKR1C1-AKR1C3 is related to different hormone dependent and independent cancers and some other diseases. The AKR1C1-3 enzymes thus represent emerging targets for the development of new drugs. Curre... |
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Electric-field triggered controlled release of bioactive volatiles from imine-based liquid crystalline phases.
Chemistry 15(1) , 117-24, (2009) Application of an electric field to liquid crystalline film forming imines with negative dielectric anisotropy, such as N-(4-methoxybenzylidene)-4-butylaniline (MBBA, 1), results in the expulsion of compounds that do not participate in the formation of the li... |
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Chemoenzymatic asymmetric total synthesis of phosphodiesterase inhibitors: preparation of a polycyclic pyrazolo[3,4-d]pyrimidine from an acylnitroso Diels-Alder cycloadduct-derived aminocyclopentenol.
J. Org. Chem. 70(7) , 2824-7, (2005) [reaction: see text] Enzymatic resolution of Boc-protected 4-aminocyclopenten-1-ol 4c gave both enantiomers 5c and 6c in high ee. Boc removal and separate condensation with chloropyrazolopyrimidine 18 provided elaborated 1,4-aminocyclopentenol derivatives 20 ... |
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Diastereoselective multicomponent cyclizations of Fischer carbene complexes, lithium enolates, and allylmagnesium bromide leading to highly substituted five- and six-membered carbocycles.
Chemistry 12(27) , 7225-35, (2006) The one-pot sequential reaction of a chromium alkoxycarbene complex, a ketone or ester lithium enolate, and allylmagnesium bromide enabled the selective synthesis of novel diastereomerically pure pentasubstituted cyclopentanols or tetrasubstituted 1,4-cyclohe... |
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Catalytic and DNA binding properties of the ogg1 protein of Saccharomyces cerevisiae: comparison between the wild type and the K241R and K241Q active-site mutant proteins.
Biochemistry 39(7) , 1716-24, (2000) The Ogg1 protein of Saccharomyces cerevisiae belongs to a family of DNA glycosylases and apurinic/apyrimidinic site (AP) lyases, the signature of which is the alpha-helix-hairpin-alpha-helix-Gly/Pro-Asp (HhH-GPD) active site motif together with a conserved ca... |
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Mass spectrometric studies of cyclopentanol derivatives in the reductive coupling of alpha,beta-unsaturated ketones assisted by samarium diiodide.
Rapid Commun. Mass Spectrom. 17(15) , 1699-702, (2003) The mass spectrometric fragmentations of a series of cyclopentanol derivatives in positive fast-atom bombardment (FAB(+)) mode were investigated. The corresponding pathways proposed were confirmed by MS/MS data obtained using linked scans at constant B/E, hig... |
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[Development of a silicon-mediated [3 + 2] annulation and its application to the synthesis of natural products].
Yakugaku Zasshi 117(6) , 368-77, (1997)
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Anomer-selective inhibition of glycosidases using aminocyclopentanols.
Org. Lett. 1(5) , 775-7, (1999) [reaction: see text] (1S,2S,3S,4R,5R)-4-amino-5-(hydroxymethyl)cyclopentane-1,2,3-triol 1 is prepared stereoselectively from D-lyxose and displays anomer-selective inhibition for beta-galactosidase (Ki = 3.0 x 10(-6) M) and beta-glucosidase (Ki = 1.5 x 10(-7)... |