Ciprofloxacin Hydrochloride
Ciprofloxacin Hydrochloride structure
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Common Name | Ciprofloxacin Hydrochloride | ||
|---|---|---|---|---|
| CAS Number | 102-92-1 | Molecular Weight | 367.802 | |
| Density | 1.199 g/cm3 | Boiling Point | 256-258 °C(lit.) | |
| Molecular Formula | C9H7ClO | Melting Point | 35-37 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | >230 °F | |
| Symbol |
GHS05 |
Signal Word | Danger | |
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Light- and temperature-responsive liposomes incorporating cinnamoyl Pluronic F127.
Int. J. Pharm. 468(1-2) , 243-9, (2014) Light- and temperature-responsive liposomes were prepared by immobilizing cinnamoyl Pluronic F127 (CP F127) on the surface of egg phosphatidylcholine liposomes. CP F127 was prepared by a condensation reaction, and the molar ratio of cinnamoyl group to Pluroni... |
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[A synthesis of cinnamoyloxyisoflavones].
Bioorg. Khim. 32(4) , 446-7, (2006) Interaction of 7-hydroxyisoflavonones with cinnamoyl chloride results in cinnamoyloxyisoflavonones. |
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Synthesis and antitumor activity of lapathoside D and its analogs
Eur. J. Med. Chem. 53 , 1-12, (2012) Phenylpropanoid sucrose esters are important class of plant-derived natural products and have greater potential to be leads for new drugs because of their structural diversity and broad-array of pharmacological and biological activities. Regio- and chemo-sele... |
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Inhibition of the β-carbonic anhydrases from Mycobacterium tuberculosis with C-cinnamoyl glycosides: identification of the first inhibitor with anti-mycobacterial activity.
Bioorg. Med. Chem. Lett. 23(3) , 740-3, (2013) A small series of C-cinnamoyl glycoside containing the phenol moiety was tested for the inhibition of the three Mycobacterium tuberculosis β-carbonic anhydrases (CAs, EC 4.2.1.1) with activities in the low micromolar range detected. The compounds were also te... |
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In vitro efficiency of 9-(N-cinnamoylbutyl)aminoacridines against blood- and liver-stage malaria parasites.
Bioorg. Med. Chem. Lett. 23(3) , 610-3, (2013) Novel 9-aminoacridine derivatives were synthesized by linking the heteroaromatic core to different cinnamic acids through an aminobutyl chain. The test compounds demonstrated mid-nanomolar in vitro activity against erythrocytic stages of the chloroquine-resis... |
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Solvent effects on the cinnamoylation of n-propyl alcohol catalyzed by N-methylimidazole and 4-dimethylaminopyridine.
J. Pharm. Sci. 72(4) , 369-72, (1983) The kinetics of reaction of trans-cinnamic anhydride or trans-cinnamoyl chloride with n-propyl alcohol, catalyzed by N-methylimidazole or 4-dimethylaminopyridine, were studied spectrophotometrically at 25 degrees in methyl ethyl ketone, ethylene dichloride, m... |
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Three-component reactions of isocyanides, dialkyl acetylenedicarboxylates, and trans-cinnamoyl chlorides for the synthesis of highly functionalized 2-vinyl furans.
Mol. Divers. 16(1) , 145-50, (2012) In this study, we present a convenient and efficient method for the synthesis of novel, highly substituted 2-vinyl furans using a three-component reaction. The zwitterions generated from the reaction of isocyanides and dialkyl acetylenedicarboxylates are reac... |
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Kinetics and mechanism of hydroxy compound cinnamoylation in acetonitrile catalyzed by N-methylimidazole and 4-dimethylaminopyridine.
J. Pharm. Sci. 72(4) , 366-9, (1983) The kinetics of reaction of the acylating agents trans-cinnamic anhydride and trans-cinnamoyl chloride with the hydroxy compounds n-propyl alcohol and water in the presence of N-methylimidazole and 4-dimethylaminopyridine were studied spectrophotometrically i... |