Ethyl chemical structure

Chemical Name 3-(4-Aminophenyl)-3-ethyl-2,6-piperidinedione Common Name 0 -(p-aminophenyl)-a-ethyl-glutarimide Structural Formula ... 

Therapeutic Function Anticholinergic, antiulcer Chemical Name Benzilic acid, 2i3iperidinoethyl ester ethobromide Common Name Piperilate ethyl bromide Structural Formula /= ... 

Mandal et al. [89-91] investigated the crystal structures of three members of the homologous series of 5-(4 -n-alkylcyclohexyl)-2-(4"-cyanophenyl)-pyrimi-dines. The crystal structures of the ethyl (ECCPP), pentyl (PCCPP), and heptyl (HCCPP) compounds were determined. The chemical structure of the compounds is presented in Fig. 15. The two lower homologues possess only a nematic phase, while the heptyl compound has a smectic phase in addition to a nematic phase. 

The term benzodiazepine refers to a specific chemical structure. Numerous benzodiazepine-receptor ligands exist which have different structures. These include the jS-carbolines (e.g. methyl-6,7-dimethoxy-4-ethyl-jS-carboline 3-carboxylate DMCM), triazolopyridazines (e.g. CL 218872), imidazopyridines (e.g. zolpidem), and pyrazolo-quinolinones (e.g. CGS 8216). In experimental animals these compounds produce... 

Figure 10.4 Chemical structures of the clinically relevant melatonin analogs, compared with melatonin (5-methoxy-N-acetyltryptamine). Agomelatine N- 2-[7-methoxy-l-naphthalenyl]ethyl)acetamide. Ramelteon ...

Sharma et al. [40] have used tetra-ethyl-ortho-silicate (TEOS) for the formation of Si02 matrix. The chemical structure of TEOS can be represented as shown in... 

Fig. 4 (a) Chemical structure of tetra-ethyl-ortho-silicate (TEOS). (b) Removal of two oxygen atoms from TEOS. (c) Mechanism depicting how TEOS chemisorbs onto silanol groups (Si-OH) on surface, (d) Formation of Si-O-Si bridges by elimination reactions with neighboring molecules. (Figure adapted from [40])... 

Although the above chemical structure is used as an example, acrylates are a class of materials rather than one single type. These polymers are formed by the copolymerisation of an acrylic ester and a cure site monomer, ethyl acrylate and chloroethyl vinyl ether respectively being illustrated above. 

Figure 9.19 Chemical structure of poly 3-[2-((S)-2-methylbutoxy)ethyl]thiophene. Number of repeating units is 50.

FIGURE 5.4 Chemical structures of photo- and electroluminescent polymers employed for polarized LEDs poly(2-methoxy-5-(2 -ethyl-hexyloxy)-p-phenylene vinylene) (MEH-PPV) poly[2,5-dioctyloxy-l, 4-diethynyl-phenylene-a/t-2,5,-bis(2 -ethylhexyloxy)-l,4-phenylene] (EHO-OPPE) poly(p-phenylene), PPP poly(3-(4-octylphenyl)-2,2 -bithiophene), PTOPT poly(p-phenylene vinylene), PPV poly(3-alkylthio-phene vinylene), P3AT Acetoxy-PPY PPV-polyester, poly(9,9-dialkyl fluorene), PF. 

The success of the carotenoid extracts led to the commercialization of synthetic carotenoids, some with the same chemical structure as those in the plant extracts and others with modifications to improve their technological properties. The yellow beta-carotene was synthesized in 1950, followed by the orange beta-8-carotenal in 1962 and the red canthaxanthin in 1964. A number of others soon followed, methyl and ethyl esters of carotenoic acid, citraxanthin, zeaxanthin, astaxanthin, and recently lutein. 

Because of their versatility and simplicity, TLC methods have been frequently applied to the separation and semi-quantitative determination of carotenoid pigments in synthetic mixtures and various biological matrices. The retention of pure carotenoid standards has been measured in different TLC systems. Separations have been carried out on silica plates using three mobile phases (1) petroleum ether-acetone, 6 4 v/v (2) petroleum ether-tert-butanol 8 2 v/v, and (3) methanol-benzene-ethyl acetate 5 75 20 v/v. Carotenoids were dissolved in benzene and applied to the plates. Developments were performed in presaturated normal chambers. The chemical structure and the Rv values of the analytes measured in the three mobile phases are listed in Table 2.1. It was concluded from the retention data that mobile phase 3 is the most suitable for the separation of this set of carotenoids [13],... 

TLC separation of the components of black dye commercial product (BDCP) was performed on silica layers. The chemical structures of the dye components are shown in Fig. 3.17. Dyes were extracted from the effluent of the dye processing plant, from the untreated river water and from the drinking water treatment plant. The organic extracts were further concentrated and purified using a copolymer of styrene divinyl benzene. The mobile phase for TLC separation consisted of toluene-ethyl acetate (8 1, v/v). The Rp values of dye components were 0.43 (C. I. Disperse Violet 93), 0.48 (C. I. Disperse Orange 37) and 0.59 (C. I. Disperse Blue 373), respectively. 

Fig. 18.6 Upper part - chemical structures of poly(oxyethylene)-segmented (POE) and amides and imides polymer derivatives (POEM). Lower left part - chemical structure of 15-crown-5-functionalized MWCNT. Lower right part - chemical structure of l-(2-acryloyloxy-ethyl)-2-methyl-benzoimidazol-l-ium iodide (AMIml).

The chemical structure for qulzalofop-ethyl Is shown below. The... 

Nizatidine Nizatidine is N-[2-[[[2-[(dimethylamino)methyl]-4-thiazolyl]methyl] thio] ethyl]-2-nitro-l,l-ethenediamine (16.2.15). According to its chemical structure, nizatidine is somewhat of a hybrid structure of ranitidine and famotidine, in which a side chain of ranitidine and carrying heterocycle, 2-aminothiazol, are used. Likewise, its synthesis also is a specific combination of pathways used for making both prototype drugs. 2-(Dimethyl-aminomethyl)-4-hydroxymethylthiazol serves as the initial compound, from which the desired nizatidine (16.2.15) is synthesized by subsequent reaction with 2-mercaptoethy-lamine hydrochloride and then with iV-methyl-l-methythio-2-nitroethenamine [71,72]. 

Encainide Encainide, 4-methoxy-N-[2-[2-(l-methyl-2-piperidinyl)ethyl]phenyl]-benza-mide (18.1.15), is synthesized by acylating 2-(l-methyl-2-piperidylethyl)aniline with 4-methoxybenzoic acid chloride. The chemical structure of encainide is substantially different than other local anesthetics and antiarrhythmics [25-27]. 

We have recently evaluated the ATRP of a wide range of hydrophilic monomers such as 2-sulfatoethyl methacrylate (SEM), sodium 4-vinylbenzoate (NaVBA), sodium methacrylate (NaMAA), 2-(dimethylamino)ethyl methacrylate (DMA), 2-(iV-morpholino)ethyl methacrylate (MEMA), 2-(diethylamino)ethyl methacrylate (DEA), oligo(ethylene glycol) methacrylate (OEGMA), 2-hydroxyethyl methacrylate (HEMA), glycerol monomethacrylate (GMA), 2-methacryl-oyloxyethyl phosphorylcholine (MPC), and a carboxybetaine-based methacrylate [CBMA]. Their chemical structures and literature references (which contain appropriate experimental details) are summarised in Table 1. 

The additives used in oxygenated gasoline are alcohols and ethers, the most common of which are ethanol (ethyl alcohol grain alcohol) and methyl t-butyl ether (MTBE). Two less commonly used additives are ethyl t-butyl ether (ETBE) and t-amyl methyl ether (TAME). The chemical structures of these four additives are shown in the diagram on page 24. 

Poly[(a-carboxymethyl)ethyl isocyanide] may be saponified with sodium hydroxide in methanol at room temperature in 5 days or at reflux in 20hrs, attended by discoloration. Aqueous solutions of the isolated salt do not show viscosities expected of polyanions. Attempt to isolate the free polycarboxylic acid by acidification is accompanied by decarboxylation, which is to be expected on the basis of its chemical structure (55). 

Fig. 10.3 Chemical structures of low affinity NMDA antagonists used for the treatment of AD, AD, AIDS dementia, and migrane. Memantine (a) Amantadine (b) (R,S)-N-2-(4-(3-thienyl)phenyl)-2-propanesulfonamide (LY392098) (c) and (R)-4 -[l-fluoro-l-methyl-2-(propane-2-sulphonylamino)-ethyl]-biphenyl-4-carboxylic acid methylamide (LY503430) (d)...

All amphetamines are synthetic, or manufactured, substances derived from alpha-methyl-beta-phenyl-ethyl-amine, a colorless liquid consisting of carbon, hydrogen, and nitrogen. In terms of their chemical structures, amphetamines are related to two natural substances known to boost energy within the human body. Those substances are ephedrine and adrenaline. Ephedrine is a natural stimulant found in plants of the genus Ephedra. It... 

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