using the resulting aldehyde‚ along with 2‚4-dimethylpyrole‚ a BODIPY dye was obtained [36]. To facilitate intersystem crossing‚ the 2- and 6- positions of the boradiazaindacene ring system were iodinated with an iodic acid-iodine mixture [37]. Bromination at the same positions was performed via N-bromosuccinamide (NBS) [38]. 8-Palmitoyl-1‚ 3‚ 5‚ 7-tetramethyl-2‚ 6 diiodo-4-bora‚ 3a‚ 4a-diaza-s-indacene was obtained by the iodination of 8-palmitoyl-1‚ 3‚ 5‚
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properties. To obtain such a pure compound‚ the compound we want must be separated from its other natural components‚ which can be done by manipulating physical and chemical properties. Panacetin contains sucrose‚ aspirin and an unknown which can be acetanilide or phenacetin in which phenacetin was created and weighed. Introduction In this lab our basic goal was to make the sucrose‚ aspirin and unknown that are formed from pharmaceutical panacetin. In doing this lab we used NaOH and diethyl either‚ along
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The objective of this lab was to identify an unknown compound by determining the melting point range using fast and slow ramps. Also‚ to determine the eutectic point of Urea and Cinnamic Acid. An unknown compound that was numbered 8 was chosen. A small amount of the unknown compound was placed in a weighing paper using a spatula. The weighing paper was folded in half twice and then was grinded using a spatula. After the unknown compound was grinded about 1-2mm was added into a capillary tube. A
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Sulfa Drugs: Preparation of Sulfanilamide Introduction The purpose of this experiment is to prepare sulfanilamide from p-Acetamidobenzenesulfonyl chloride. This will be done using reflux‚ vacuum filtration‚ and melting point determination. Experiment Scheme6 Figure 1. Reaction equation.6 A hot water bath was prepared in a fume hood using a 250-mL beaker. 2.5 g of p-acetamidobenzenesulfonyl chloride was placed into a 50 mL Erlenmeyer flask and 11 mL of dilute ammonium hydroxide solution
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To get to aniline‚ tin metal acts as a reducing agent and is oxidized to SnCl4. The purification of crude aniline is done by distillation and extraction. Aniline can be converted to acetanilide by acetylation reaction using acetic anhydride with sodium acetate. This step protects the amine functional group from doing unwanted reactions during chlorosulfonation and amination steps. The chlorosulfonyl group attacks in the para position
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Separating The Components of “Panacetin” Observations Most natural products and many commercial preparations are mixtures containing a number of different substances. To obtain a pure compound from such a mixture‚ you must separate the desired compound from the other components of the mixture by taking advantage of differences in their physical and chemical properties. Acidic or basic substances are often converted to water-soluble salts‚ which can then be separated from the water-insoluble
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melting point which should be around 240 ºC along with a flame test which should be green-blue. CHEMICAL PROPERTIES TABLE See Attached Lab Notebook Copies REACTION MECHANISM In this lab we used multiple techniques to complete and verify the bromination of trans-stilbene. First technique we used was to reflux the mixture; this contains having the mixture boiling so it will evaporate while the condenser will recondense the solvent which is boiling off so the solvent may stay in the reaction. Next
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Subject: Experiment 23: Stereochemistry of the Addition of Bromine to trans-Cinnamic Acid Introduction/Abstract: The purpose of this experiment was to carry out the bromination of trans-cinnamic acid‚ to determine the stereochemistry of the dibromide product of 2‚3-dibromo-3-phenylpropanoic acid‚ and find out whether the reaction proceeds by the usual bromonium ion mechanism or some other mechanism. In this experiment trans-cinnamic acid was mixed with glacial acetic acid and stirred in which
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Experimental Synthesis of Bupropion – A round bottom flask (RBF) containing m-chloropropiophenone (1.0 g‚ 5.9 mmol) dissolved in 5.0 mL dichloromethane (DCM) with 0.25 mL of 1.0 M Br2 in DCM was briefly warmed to initiate the bromination reaction. Afterwards‚ the RBF was placed in and ice-water bath and 1.0 M Br2 in DCM (6.0 mL‚ 6.25 mmol) was added dropwise while stirring. DCM was removed from the reaction by rotary evaporation. Next‚ tert-butylamine (5.0 mL‚ 47.6 mmol) and 5.0 mL of N-methylpyrrolidinone
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a boiling chip to any liquid before heating it. • Always wear department approved eye goggles at all times. • Long pants and closed toe shoes are required. Table of Reagents Reagent Mol. Wt. (g/mol) Bp ( ͦ C) Mp ( ͦ C) Density (g/ml) Acetanilide 135.17 304 113-115 1.219 Fluorene
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