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1,2-Dimethylcyclopentane | CAS:2452-99-5
1,2-Dimethylcyclopentane
  • Name:1,2-Dimethylcyclopentane
  • CAS:2452-99-5
  • Synonyms:
  • Molecular Formula:C7H14
  • Molecular Weight:98.19
  • EINESC:219-520-6

Description

Properties

Melting point -119.1 ºC***
Boiling point 94-99 ºC (760 Torr)**
Flash point -5.6±11.7 ºC, 计算值*
Density 0.764 g/cm3 (20 ºC)**
Refractive index 1.41745 (589.3 nm 20 ºC)***

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SDS

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Articles
Peer-Reviewed Papers
Metabolism of carcinogenic urethane to nitric oxide is involved in oxidative DNA damage.Katsuhisa Sakano et al.Free radical biology & medicine, 33(5), 703-714 (2002-09-05) Metabolism of N-hydroxyurethane by guinea pig liver preparations.K Tatsumi et al.Journal of pharmacobio-dynamics, 5(11), 916-920 (1982-11-01) Induction of chromosome breaks in cultured normal human leukocytes by potassium arsenite, hydroxyurea and related compounds.J J Oppenheim et al.Cancer research, 25(7), 980-985 (1965-08-01) Timing of chemically induced neoplasia in mice revealed by the antineoplastic action of caffeine.T Nomura Cancer research, 40(4), 1332-1340 (1980-04-01) DNA repair synthesis induced by N-hydroxyurea, acetohydroxamic acid, and N-hydroxyurethane in primary rat hepatocyte cultures: comparative evaluation using the autoradiographic and the bromodeoxyuridine density-shift method.S Rossberger et al.Mutation research, 145(3), 201-207 (1985-05-01) Kinetic applications of electron paramagnetic resonance spectroscopy. 28. N-Alkoxy-N-alkylamino, N-alkoxyamino, and N-alkoxyanilino radicals.Kaba RA and Ingold KU Journal of the American Chemical Society, 98(23), 7375-7380 (1976) N-hydroxycarbamate is the substrate for the pyruvate kinase catalyzed phosphorylation of hydroxylamine.P M Weiss et al.Biochemistry, 23(19), 4346-4350 (1984-09-11) Enhanced antibacterial effect of silver nanoparticles obtained by electrochemical synthesis in poly(amide-hydroxyurethane) media.Marius Stefan et al.Journal of materials science. Materials in medicine, 22(4), 789-796 (2011-03-29) Involvement of liver aldehyde oxidase in conversion of N-hydroxyurethane to urethane.K Sugihara et al.Journal of pharmacobio-dynamics, 6(9), 677-683 (1983-09-01) Comparative carcinogenicities and mutagenicities of vinyl carbamate, ethyl carbamate, and ethyl N-hydroxycarbamate.G A Dahl et al.Cancer research, 40(4), 1194-1203 (1980-04-01) Immunotoxicity of ethyl carbamate in female BALB/c mice: role of esterase and cytochrome P450.S W Cha et al.Toxicology letters, 115(3), 173-181 (2000-05-18) Rodent species and strain specificities for sister-chromatid exchange induction and gene mutagenesis effects from ethyl carbamate, ethyl N-hydroxycarbamate, and vinyl carbamate.Y Sharief et al.Mutation research, 126(2), 159-167 (1984-04-01) Antiteratogenic effects of tumor inhibitors, caffeine, antipain, and retinoic acid in mice.T Nomura et al.Cancer research, 43(11), 5156-5162 (1983-11-01)
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