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Cyclooctanol | CAS:696-71-9
Cyclooctanol
  • 名称:环辛醇 | Cyclooctanol
  • CAS号:696-71-9
  • 别名:
  • 分子式:C8H16O
  • 分子量:128.21
  • EINESC号:211-800-6

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物理化学性质

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Binding of triethyltin bromide to cat haemoglobin.K R Siebenlist et al.The Biochemical journal, 233(2), 471-477 (1986-01-15) From the Cover: Developmental Neurotoxicants Disrupt Activity in Cortical Networks on Microelectrode Arrays: Results of Screening 86 Compounds During Neural Network Formation.Christopher L Frank et al.Toxicological sciences : an official journal of the Society of Toxicology, 160(1), 121-135 (2017-10-04) Inactivation of yeast hexokinase B by triethyltin bromide.K R Siebenlist et al.Biochemistry, 22(18), 4229-4234 (1983-08-30) Triethyltin-produced decrease and recovery of wheel running and food-reinforced lever pressing in rats.G J Gerber et al.Neurobehavioral toxicology and teratology, 7(5), 433-438 (1985-09-01) The effect of temperature on the inhibition of trout, carp and human red cell hexokinase by triethyltin bromide.K R Siebenlist et al.Comparative biochemistry and physiology. C: Comparative pharmacology, 70(2), 261-264 (1981-01-01) Peripheral and central nervous system lesions caused by triethyl- and trimethyltin salts in rats.D J O'Shaughnessy et al.Toxicologic pathology, 14(2), 141-148 (1986-01-01) New links between SOD1 and metabolic dysfunction from a yeast model of amyotrophic lateral sclerosis.Emma L Bastow et al.Journal of cell science, 129(21), 4118-4129 (2016-11-03) The metabolism and toxicity of some organotin compounds in isolated rat hepatocytes.P Wiebkin et al.Toxicology and applied pharmacology, 62(3), 409-420 (1982-03-15) Trimethyltin exposure produces an unusual form of toxic auditory damage in rats.J S Young et al.Toxicology and applied pharmacology, 82(1), 87-93 (1986-01-01) Histopathology of spinal cord, peripheral nerve, and soleus muscle of rats treated with triethyltin bromide.E A Richman et al.Experimental neurology, 86(1), 122-133 (1984-10-01) Inactivation of yeast hexokinase B by triethyltin bromide and reactivation by dithiothreitol and glucose.K R Siebenlist et al.Biochemistry, 22(20), 4642-4646 (1983-09-27)
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