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Physical Constants of Organic Compounds
Published in W. M. Haynes, David R. Lide, Thomas J. Bruno, CRC Handbook of Chemistry and Physics, 2016
W. M. Haynes, David R. Lide, Thomas J. Bruno
Name 2,4-Pentanedione Pentanoic acid 1-Pentanol 2-Pentanol 2-Pentanone 3-Pentanone 1-Pentene Pentyl acetate Pentylamine Perylene Phenanthrene Phenol Phthalic acid Phthalic anhydride -Pinene -Pinene Piperidine Propanal Propane 1,3-Propanediol Propanenitrile Propanoic acid 1-Propanol 2-Propanol Propene Propyl acetate Propylbenzene Propyl formate Propyl propanoate Pyrazine Pyrene Pyridine Pyrimidine Pyrocatechol Pyrrole Pyrrolidine Quinoline Resorcinol Safrole Salicylaldehyde Octadecanoic acid Styrene Succinic acid Succinic anhydride Mol. form. C5H8O2 C5H10O2 C5H12O C5H12O C5H10O C5H10O C5H10 C7H14O2 C5H13N C20H12 C14H10 C6H6O C8H6O4 C8H4O3 C10H16 C10H16 C5H11N C3H6O C3H8 C3H8O2 C3H5N C3H6O2 C3H8O C3H8O C3H6 C5H10O2 C9H12 C4H8O2 C6H12O2 C4H4N2 C16H10 C5H5N C4H4N2 C6H6O2 C4H5N C4H9N C9H7N C6H6O2 C10H10O2 C7H6O2 C18H36O2 C8H8 C4H6O4 C4H4O3 -m/10-6 cm3 mol-1 54.9 66.5 67.0 69.1 57.5 57.7 54.6 88.9 69.3 167.5 127.6 60.6 83.6 66.7 100.7 101.9 64.2 34.2 38.6 50.2 38.6 43.5 45.2 45.7 30.7 65.9 89.1 55.0 77.7 37.8 147 48.7 43.1 68.2 48.6 54.8 86.1 67.2 97.5 66.8 220.8 68.2 58.0 47.5 -/10-6 0.533 0.608 0.619 0.634 0.540 0.542 0.499 0.598 0.600 0.896 0.702 0.679 1.097 0.688 0.631 0.643 0.649 0.510 0.432* 0.695 0.548 0.580 0.601 0.594 0.368* 0.569 0.637 0.566 0.586 0.487 0.924 0.605 0.581 0.832 0.703 0.662 0.732 0.780 0.661 0.639 0.730 0.590 0.772 0.570 Name Terephthalic acid o-Terphenyl m-Terphenyl p-Terphenyl 1,1,2,2-Tetrabromoethane Tetrabromomethane 1,1,2,2-Tetrachloroethane Tetrachloroethene Tetrachloromethane Tetradecane Tetradecanoic acid Tetrahydrofurfuryl alcohol Tetraiodomethane 1,2,4,5-Tetramethylbenzene Tetranitromethane Thiophene Toluene o-Toluic acid m-Toluic acid p-Toluic acid Tribromomethane Trichloroacetaldehyde Trichloroacetic acid Trichloroethene Trichlorofluoromethane Trichloromethane Trichloronitromethane Tridecane Triethylamine Trifluoroacetic acid Triiodomethane 1,3,5-Trimethylbenzene 2,2,4-Trimethylpentane 2,3,4-Trimethylpentane 2,4,6-Trimethylpyridine Undecane Urea Vinyl acetate Vinyl formate o-Xylene m-Xylene p-Xylene
Physical Properties of Individual Groundwater Chemicals
Published in John H. Montgomery, Thomas Roy Crompton, Environmental Chemicals Desk Reference, 2017
John H. Montgomery, Thomas Roy Crompton
Uses: Disinfectant; phenolic resins; tricresyl phosphate; ore flotation; textile scouring agent; organic intermediate; manufacturing salicylaldehyde, coumarin, and herbicides; surfactant; synthetic food flavors (para isomer only); food antioxidant; dye, perfume, plastics, and resins manufacturing.
A review on ‘sulfonamides’: their chemistry and pharmacological potentials for designing therapeutic drugs in medical science
Published in Journal of Coordination Chemistry, 2023
Wardha Zafar, Sajjad Hussain Sumrra, Abrar Ul Hassan, Zahid Hussain Chohan
Metal complexes of halogen substituted Schiff bases show remarkable antimicrobial properties. Salicylaldehyde derivatives containing one or more halogen atoms revealed potential for biological activities such as antifungal, antitumor and antibacterial. In view of previous findings, Anandakumaran et al. [87] reported the synthesis of 3,5-dichlorosalicylaldehyde derived sulfanilamide Schiff base (L) along with six divalent 3d-metal complexes (9a-9f) (Scheme 9). For antibacterial activity, the values of minimum inhibition concentration (MIC) for the streptomycin (reference drug) and synthesized compounds were 6-12.5 μg/mL and 20-150 μg/mL, respectively. The antibacterial activities revealed that the M(II) complexes have greater antibacterial potential but less than that of streptomycin against all the tested bacterial species. From this series, Hg(II) complex 9b was the most active compound with highest inhibition zone of 14 mm against S. aureus. For antifungal activity, the MIC values for amphotericin B (reference drug) and compounds were 0.03-16 μg/mL and 20-100 μg/mL, respectively.
Synthesis, characterization, crystal structure, and electrochemical properties of three copper(II) complexes with 3,5-dihalosalicylaldehyde Schiff bases derived from amantadine
Published in Journal of Coordination Chemistry, 2019
Xu-Dong Jin, Han Wang, Xiao-Kang Xie, Jia-Yue Sun, He-Ming Liang
In many countries, amantadine (SymmetrelTM) and rimantadine (FlumadineTM) have been widely used to treat or prevent seasonal influenza as efficacious remedies [14–17]. It can also alleviate Parkinson symptoms [18, 19]. Salicylaldehyde and substituted salicylaldehydes, especially halogenated salicylaldehydes, were used to produce herbicides, insecticides and fungicides [20–22]. As an extension of our previous studies on the electrochemical properties of copper complexes with Schiff bases derived from amantadine or rimantadine [23, 24], we designed and synthesized three copper(II) complexes with the Schiff bases derived from amantadine and 3,5-dihalosalicylaldehydes.