
1-Acetyl-1-hydroxycyclohexane | CAS:1123-27-9
1-Acetyl-1-hydroxycyclohexane
- Name:1-Acetyl-1-hydroxycyclohexane
- CAS:1123-27-9
- Synonyms:1-Acetylcyclohexanol; 1-Hydroxycyclohexyl methyl ketone; NSC 31427; NSC 37640
- Molecular Formula:C8H14O2
- Molecular Weight:142.20
- EINESC:214-372-9
Description
Properties
Boiling point | 125.5 ºC*** |
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Flash point | 95.9±15.2 ºC, 计算值* |
Density | 1.0248 g/cm3 (25 ºC)** |
Refractive index | 1.4738 (589.3 nm 25 ºC)**** |
Safety
没有数据 | 没有数据 |
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SDS
Source | SDS/MSDS Samples |
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没有数据 | 没有数据 |
Synthetic Route
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More
Articles
Peer-Reviewed Papers
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Synthesis and antituberculosis activity of some new pyridazine derivatives. Part II.Dorina Mantu et al.European journal of medicinal chemistry, 45(11), 5164-5168 (2010-09-04)
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Synthesis, molecular modelling and anticancer evaluation of new pyrrolo[1,2-b]pyridazine and pyrrolo[2,1-a]phthalazine derivativesPopovici L, et al. Journal of Enzyme Inhibition and Medicinal Chemistry, 34(1), 230-243 (2019)
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2-Phenylimidazo[1,2-b]pyridazine derivatives highly active against Haemonchus contortus.Abdelselam Ali et al.Bioorganic & medicinal chemistry letters, 21(14), 4160-4163 (2011-06-21)
4-Hydroxypyridazin-3(2H)-one derivatives as novel D-amino acid oxidase inhibitors.Takeshi Hondo et al.Journal of medicinal chemistry, 56(9), 3582-3592 (2013-04-10)
Lead optimization of a sulfonylurea-based piperazine pyridazinone series of glucan synthase inhibitors.Andrew J Zych et al.Bioorganic & medicinal chemistry letters, 22(14), 4896-4899 (2012-06-13)
Aminothienopyridazine inhibitors of tau aggregation: evaluation of structure-activity relationship leads to selection of candidates with desirable in vivo properties.Carlo Ballatore et al.Bioorganic & medicinal chemistry, 20(14), 4451-4461 (2012-06-22)
Response of chronic gingivitis to hygiene therapy and experimental gingivitis. Clinical, microbiological and metabonomic changes.Malgorzata Klukowska et al.American journal of dentistry, 28(5), 273-284 (2015-12-31)
Synthesis and biological evaluation of new heteroaryl carboxylic acid derivatives as anti-inflammatory-analgesic agents.Khaled Abouzid Mohamed Abouzid et al.Chemical & pharmaceutical bulletin, 61(2), 222-228 (2013-02-02)
A new and efficient synthetic route for the anxiolytic agent CL285032.Victor P Ghidu et al.Bioorganic & medicinal chemistry letters, 21(1), 259-261 (2010-11-26)
A modular synthesis of teraryl-based α-helix mimetics, part 2: Synthesis of 5-pyridine boronic acid pinacol ester building blocks with amino acid side chains in 3-position.Martin Peters et al.Chemistry (Weinheim an der Bergstrasse, Germany), 19(7), 2450-2456 (2013-01-03)
The diazines: Pyridazine, pyrimidine, and pyrazine: reactions and synthesis Heterocyclic Chemistry (2013)
A Raman study on preferential interactions in the formamide/pyridine/pyridazine system and complementary thermodynamic information on the formamide/pyridazine mixture.Elaine F da Silva et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 102, 71-74 (2012-12-12)
Six membered heterocyclic compounds with two or more heteroatoms Heterocyclic Chemistry (2010)
Pyridazine based scorpionate ligand in a copper boratrane compound.Gernot Nuss et al.Inorganic chemistry, 50(24), 12632-12640 (2011-11-19)
Structural insight for imidazopyridazines as malarial kinase PfPK7 inhibitors using QSAR techniques.Nitendra K Sahu et al.Medicinal chemistry (Shariqah (United Arab Emirates)), 8(4), 636-648 (2012-04-26)
Bromopyridazinedione-mediated protein and peptide bioconjugation.Vijay Chudasama et al.Chemical communications (Cambridge, England), 47(31), 8781-8783 (2011-07-09)
Discovery of a novel class of orally active antifungal beta-1,3-D-glucan synthase inhibitors.Scott S Walker et al.Antimicrobial agents and chemotherapy, 55(11), 5099-5106 (2011-08-17)
Isomer Dependence on the Reactivity of Diazenes with Pentaphenylborole.Venkata A K Adiraju et al.Chemistry (Weinheim an der Bergstrasse, Germany), 23(47), 11437-11444 (2017-07-05)
N-Phenyl-4-pyrazolo [1, 5-b] pyridazin-3-ylpyrimidin-2-amines as potent and selective inhibitors of glycogen synthase kinase 3 with good cellular efficacyTavares FX, et al. Journal of Medicinal Chemistry, 47(19), 4716-4730 (2004)
Anti-inflammatory effect and selectivity profile of AS1940477, a novel and potent p38 mitogen-activated protein kinase inhibitor.Masaomi Terajima et al.European journal of pharmacology, 698(1-3), 455-462 (2012-11-28)
Electrochemical, computational, and photophysical characterization of new luminescent dirhenium-pyridazine complexes containing bridging OR or SR anions.Alessio Raimondi et al.Inorganic chemistry, 51(5), 2966-2975 (2012-03-01)
Determination of liquid chromatography/flame ionization detection response factors for N-heterocycles, carboxylic acids, halogenated compounds, and others.Christian Becker et al.Analytical and bioanalytical chemistry, 412(1), 171-179 (2019-12-14)
Electron stimulated desorption from condensed pyrimidine and pyridazine.L Ellis-Gibbings et al.Physical chemistry chemical physics : PCCP, 19(20), 13038-13048 (2017-05-10)
Hydrogen bonding and reactivity of water to azines in their S1 (n,π*) electronic excited states in the gas phase and in solution.Jeffrey R Reimers et al.Physical chemistry chemical physics : PCCP, 14(25), 8791-8802 (2012-04-26)
Using Voltammetry to Measure the Relative Hydrogen-Bonding Strengths of Pyridine and Its Derivatives in Acetonitrile.Malcolm E Tessensohn et al.Chemphyschem : a European journal of chemical physics and physical chemistry, 18(16), 2250-2257 (2017-06-14)
Shape and core excited resonances in electron collisions with diazines.Zdeněk Mašín et al.The Journal of chemical physics, 137(20), 204312-204312 (2012-12-05)
Discovery and optimization of potent and selective imidazopyridine and imidazopyridazine mTOR inhibitors.Emily A Peterson et al.Bioorganic & medicinal chemistry letters, 22(15), 4967-4974 (2012-07-07)
Pyridazine-derived γ-secretase modulators.Zehong Wan et al.Bioorganic & medicinal chemistry letters, 21(13), 4016-4019 (2011-06-04)
Synthesis and antiproliferative effects of 5,6-disubstituted Pyridazin-3(2H)-ones designed as conformationally constrained combretastatin A-4 Analogues.Mohamed Elagawany et al.Anti-cancer agents in medicinal chemistry, 13(7), 1133-1140 (2013-04-12)
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