ester (Also esters) : Related Words Words similar in meaning to ester

  • plasticizer«
  • organic matter«
  • glyceride«
  • chemistry«
  • ester«
  • glyceryl ester«
  • cellulose ester«
  • ethyl acetate«
  • nucleotide«
  • cyclohexanol phthalate«
  • lactate«
  • citrate«
  • polyester«
  • maleate«
  • urethane«
  • banana oil«
  • base«
  • glycerol tristearate«
  • glycerol tripalmitate«
  • glycerol trimargarate«
  • cellulose acetate«
  • adenylic acid«
  • cellulose xanthate«
  • cellulose nitrate«
  • uracil«
  • adenosine triphosphate«
  • adenosine monophosphate«
  • adenosine diphosphate«
  • deoxythymidine monophosphate«
  • deoxyguanosine monophosphate«
  • deoxycytidine monophosphate«
  • deoxyadenosine monophosphate«
  • nitrocellulose«
  • glycerin jelly«
  • viscose«
  • guncotton«
  • stearin«
  • base pair«
  • tristearin«
  • tripalmitin«
  • triolein«
  • palmitin«
  • nitrocotton«
  • muton«
  • margarin«
  • glycerole«
  • glycerogelatin«
  • glycerogel«
  • glycerite«
  • butyrin«
  • acylglycerol«
  • olein«
  • silicon ester«
  • carboxylic acid«
  • esterify«
  • cellulose triacetate«
  • jojoba ester«
  • alcohol«
  • rco2r′«
  • triglyceride«
  • esterification«
  • r′oh«
  • chemical science«
  • zoledronate«
  • reaction«
  • triacetate«
  • xylate«
  • phosphorus–oxygen double bond«
  • xylarate«
  • carbon–oxygen–phosphorus bonding«
  • tributyrin«
  • xanthoproteate«
  • amide«
  • pyroxyline«
  • xanthate«
  • carbonyl«
  • pyroxylin«
  • wax«
  • acid«
  • pyrocellulose«
  • water«
  • inorganic chemistry«
  • voacangine«
  • rco2h«
  • organic compound«
  • verbascoside«
  • inorganic acid«
  • organic chemistry«
  • vanillate«
  • transesterification«
  • chemist«
  • vanadite«
  • deprotonation«
  • geochemistry«
  • valproate pivoxil«
  • orthoesters«
  • chemical«
  • valproate«
  • butyl ester«
  • pill roller«
  • valerate«
  • aldehyde«
  • pill pusher«
  • ursolate«
  • amine«
  • pharmacist«
  • ursodeoxycholate«
  • acyl chloride«
  • surface chemistry«
  • uronate«
  • ether«
  • physical chemistry«
  • urocanate«
  • acid anhydride«
  • nuclear chemistry«
  • unoprostone«
  • oxygen«
  • electrochemistry«
  • undecylenate«
  • phosphorus–carbon bond«
  • druggist«
  • undecenoate«
  • central inorganic atom«
  • photochemistry«
  • undecanoate«
  • rco2ch3«
  • apothecary«
  • tyropanoate«
  • ester analog«
  • radiochemistry«
  • tungstosilicate«
  • method«
  • thermochemistry«
  • tryptophanate«
  • stronger nucleophiles«
  • immunochemistry«
  • tristearate«
  • many ester«
  • femtochemistry«
  • triphosphoric acid«
  • hydrogen«
  • chemoimmunology«
  • triphosphate«
  • parent alcohol«
  • trimyristin«
  • organic ester«
  • trimethylolethane«
  • alkene«
  • trihydroxybenzoate«
  • typical catalyst«
  • fischer esterification«
  • trifluoromethylbenzoate«
  • presence«
  • trifluoroacetate«
  • sulfuric acid«
  • triflate«
  • claisen condensation«
  • triester«
  • fragrance«
  • trichloroacetate«
  • fatty acid ester«
  • tricarboxylate«
  • organolithium compound«
  • tricarballylate«
  • tricaine«
  • diazomethane«
  • tributyl phosphate«
  • alkoxides«
  • tribromoacetate«
  • peptide synthesis«
  • alkoxide«
  • tosylate«
  • catalytic hydrogenation«
  • titanate«
  • ch3oh«
  • tiludronate«
  • methyl ester«
  • threonate«
  • borate«
  • thiosulfuric acid«
  • organophosphate«
  • thiosulfate«
  • alkyl halide«
  • thionate«
  • thioglycolate«
  • nucleophiles«
  • thioester«
  • reaction product«
  • thiocyanic acid«
  • ethylene glycol«
  • thiocyanate«
  • carbonic acid«
  • thiobenzoate«
  • nitrile«
  • thioate«
  • agent«
  • thioacetate«
  • gas chromatography«
  • tetronate«
  • basic condition«
  • tetrolate«
  • acidic condition«
  • tetramate«
  • phosphoric acid«
  • tetraethylorthosilicate«
  • glycerol«
  • tetradecanoate«
  • strong base«
  • tetraacetate«
  • oxygen atom«
  • terephthalate«
  • essential oil«
  • taurodeoxycholate«
  • acetic acid«
  • taurocholate«
  • taurochenodeoxycholate«
  • ketone«
  • taurate«
  • conformation«
  • tartrate«
  • fatty acid«
  • tannate«
  • mixture«
  • sylvate«
  • hydrolysis«
  • sultone«
  • dehydration«
  • sultine«
  • physical property«
  • sulphotungstate«
  • odor«
  • sulphostannate«
  • –o–alkyl«
  • sulphocyanate«
  • νc=o.«
  • sulpharsenate«
  • welchen eine säure mit einem aether verbunden ist«
  • sulfonate«
  • wasser oder«
  • sulfomucin«
  • volatile ether compound«
  • sulfometuron«
  • viele mineralische«
  • sulfolipid«
  • verbindungen von alkohol«
  • sulfinate«
  • sulfur ester«
  • sulfate«
  • sulfate esters/organosulfates«
  • sulfanilate«
  • silver carboxylate«
  • sulfamate«
  • sequesters water«
  • sugar phosphate«
  • salze betrachten kann«
  • sucroglyceride«
  • succinylase«
  • rconhr″«
  • succinate«
  • suberate«
  • styphnate«
  • phosphate esters/organophosphates«
  • stovain«
  • o–c–o angle«
  • stearate«
  • original text:b«
  • squarate«
  • organophosphites«
  • sorbate«
  • organische sauerstoffsäuren treten mit einer alkohol«
  • sinapine«
  • op(c6h5)3«
  • sinapate«
  • nucleophilic enolate«
  • silicotungstate«
  • sialate«
  • nach der radicaltheorie«
  • selenoester«
  • methanol yield methyl formate«
  • selenocyanate«
  • metal–acyl complex«
  • selenite«
  • iupac nomenclature methanoate«
  • selenate«
  • intramolecular equivalent«
  • sebacate«
  • intermediate hydroxamic acid«
  • sarcosinate«
  • intermediate hemiacetal«
  • saponify«
  • intense sharp band«
  • saponification«
  • inorganic oxo acid«
  • sapintoxin«
  • inorganic esters«
  • santoninate«
  • inorganic acid ester«
  • salophen«
  • hydrolysation«
  • salicylate«
  • hexyl caprylate«
  • saccharonate«
  • hc(oh)3«
  • saccharinate«
  • german essigäther«
  • saccharate«
  • formula ch3(ch2)6co2(ch2)5ch3«
  • rosmarinate«
  • form rco2r′«
  • risedronate«
  • flüchtigen ätherischen verbindungen zusammen«
  • ricinoleate«
  • ricinolate«
  • ether du troisième genre«
  • ricinelaidate«
  • ester odorants«
  • rhodizonate«
  • ester oder sauerstoffsäure aetherarten«
  • retinoate«
  • ester name«
  • reesterify«
  • ester hexyl octanoate«
  • racemate«
  • dipole minimization effect«
  • quinolinate«
  • degrading triglyceride«
  • pyruvate«
  • c–o–c bond«
  • pyrotartrate«
  • c–c–o«
  • pyrophosphate«
  • complex carboxylic acid«
  • pyromucate«
  • ch3o2ch«
  • pyromalate«
  • ch3cooc4h9«
  • pyroglutamate«
  • ch3co2c4h9«
  • pyrocarbonate«
  • central inorganic sulfur atom«
  • propylparaben«
  • carbon–oxygen–central inorganic atom covalent bond«
  • propionate«
  • c6h4)(co2ch3)2«
  • propiolate«
  • c6h4)(co2)2(c2h4)}n«
  • propenoate«
  • c2h5co2r«
  • propanoate«
  • c2h3o2cch3«
  • prolinate«
  • buoac«
  • prephenate«
  • bifunctional amino acid«
  • prednimustine«
  • art unter ausscheidung von wasser zu«
  • polythionate«
  • anion availability«
  • polyphosphoester«
  • analogous acylation«
  • polymethacrylate«
  • acid ether«
  • polyglycerol«
  • acetic ether«
  • polyesteramide«
  • β-hydrogen atom«
  • polyaminopolycarboxylate«
  • α-hydroxyl«
  • polyalkenoate«
  • uncommon class«
  • polyadenylate«
  • typical ester«
  • polyacrylate«
  • triethylorthoformate«
  • platinocyanate«
  • pivoxazepam«
  • thiosulfonates«
  • pivampicillin«
  • systematic iupac«
  • pivalate«
  • suffix -oate«
  • pirisudanol«
  • specific ester«
  • pipecolate«
  • specialized organic synthetic operation«
  • pinate«
  • polyolester«
  • pimelate«
  • polymeric sulfonic acid«
  • pimarate«
  • hydroxyarylketones«
  • picrate«
  • hc(oc2h5)3«
  • picramate«
  • formula rc(or′)3«
  • picolinate«
  • fine chemical synthesis«
  • phytate«
  • dibah«
  • phthalate«
  • c–h bond adjacent«
  • phosphotungstate«
  • butyl ethanoate«
  • phosphoserine«
  • ammonolysis reaction«
  • phosphopantetheinylate«
  • h2o«
  • phosphonoacetate«
  • z conformation«
  • phosphonate«
  • triesters«
  • phospholipase«
  • scale procedure«
  • phosphoglyceric acid«
  • rco)2o«
  • phosphodiester«
  • phosphoesters«
  • phosphocholine«
  • metal carbonyl catalyst«
  • phosphite«
  • german chemist leopold gmelin«
  • phosphate«
  • ethanoate«
  • phosphatase«
  • chan rearrangement«
  • phocenate«
  • phloretin«
  • nomenclature«
  • phenylpropionate«
  • säuren«
  • phenyllactate«
  • organic carbonate«
  • phenylacetate«
  • oligoester«
  • phenpropionate«
  • hydroesterification«
  • phenetsal«
  • fráter–seebach alkylation«
  • phenate«
  • ester moiety«
  • pertechnate«
  • carbonylation«
  • peroxynitrate«
  • borinic ester«
  • peracetate«
  • sulfinates«
  • pentonate«
  • simplest carboxylic acid«
  • pentetate«
  • pentagalloylglucose«
  • rcocl«
  • pentagalacturonate«
  • rch2oh«
  • pentadienoate«
  • poly(ethylene terephthalate«
  • pentadecanoate«
  • phosphinites«
  • penamecillin«
  • orthoformic acid«
  • pectinate«
  • hydride source«
  • pantothenate«
  • ester pyrolysis«
  • pantoate«
  • pamoate«
  • characterization«
  • pamidronate«
  • form adduct«
  • palmitoylcarnitine«
  • carboxylate salt«
  • palmitostearate«
  • palmitoleate«
  • α-haloketones«
  • palmitate«
  • steglich esterification«
  • palmate«
  • stark apparatus«
  • similar molecular weight«
  • oxopropanoate«
  • phosphonites«
  • oxoglutarate«
  • oxalocrotonate«
  • esterifications«
  • oxaloacetate«
  • classic synthesis«
  • oxalate«
  • cellulolysis«
  • orthosilicic acid«
  • carbon–oxygen bond«
  • orthosilicate«
  • baeyer–villiger oxidation«
  • orthophosphate«
  • acrylate ester«
  • orsellinate«
  • phenyl ester«
  • orotate«
  • low polarity«
organosulfate, ethanoic acid, copper chromite, butanoate, oleocanthal, γ-valerolactone, oleate, triphenyl phosphate, oilfish, thiosulfinates, octyl gallate, their flexibility, octocrylene, cyclic ester, octanol, cyanate ester, octanoate, catalyst, octadecenoate, octadecadienoate, phosphite ester, norbixin, lossen rearrangement, nonester, triethylsilane, nitrous acid, distinctive fruit, nitroglycerine, nitrite, main commercial source, nitrilotriacetate, iodide salt, nitrate, boronic ester, nicotinate, nucleophilic abstraction, nicomorphine, neuraminate, carbonyl center, naphthoate, bouveault–blanc reduction, naphthenate, azeotropes, nalidixate, alternative presentation, myronate, strong nucleophiles, myristoleate, parent acid, myristate, nitrate ester, mucate, carbon nucleophiles, morrhuate, vinyl alcohol, monophosphothiamine, conformational isomerism, monomethylfumarate, pinner reaction, monolaurate, malonic ester synthesis, monohydroxybenzoate, dieckmann condensation, monoglyceride, dicyclohexylcarbodiimide, monoglutamate, fry rearrangement, monoester, carboxylic, monodehydroascorbate, bond donor, minodronate, bond acceptor, mevalonate, transfer catalyst, metrizoate, dimethyl terephthalate, methylsalycylate, nature, methylparaben, proton source, methylmalonate, fruity odor, methylitaconate, flavor industry, methylesterase, favorskii rearrangement, methyl salicylate, ethylene carbonate, methyl methacrylate, carboxylate anion, methyl formate, polar aprotic solvent, methyl acrylate, carbon adjacent, methyl acetate, anodic oxidation, methyacrylate, alkyl chloride, methoxycinnamate, methoxycarbonyl, finkelstein reaction, methanoate, alcoholysis, methanesulfonate, trivial name, methacrylate, many mineral, metaphosphate, –oh, metaborate, elimination, mesitoate, methyl ketone, melissate, mitsunobu reaction, medium-chain triglyceride, explosive property, meconate, butyl acetate, margarate, phase transfer catalyst, mannonate, quantitative yield, malvalate, aqueous acid, malonate, anhydrous condition, maleylpyruvate, malonic acid, malate, dmap, lysophosphatidate, lower boiling, lycopenoate, hyperconjugation, lithospermate, direct reduction, lipoate, isobutylene, linoleic, diester, linoleate, ch3co2h, levulinate, alkoxy, levophacetoperane, ir spectrum, lecanorate, salt, laurate, artificial flavoring, lantanurate, lactylate, sodium methoxide, lactone, ozonolysis, lactoglyceride, trans, butyrate, kynurenate, kojate, silver ion, ketovalerate, cyclic structure, ketopimelate, carbonyl oxygen, ketonization, ketoisovalerate, ketoisocaproate, sulfites, ketoglutarate, fatty alcohol, ketogluconate, low barrier, ketoester, other reaction, ketocarboxylate, reversible reaction, ketobutyrate, phosphorus atom, ketoadipate, vinyl acetate, kainate, ester bond, jasmonic acid, molecular sieve, jasmonate, lower melting, jalapinolate, le chatelier, jalapate, lactones, itaconate, hydroxylamine, isovaleric acid, ethyl ester, isovalerate, carbonyl carbon, isothiocyanate, reduction, isosaccharinate, lithium aluminium hydride, isophthalate, propionic acid, isomerohydrolase, isocyanate, isocyanurate, iupac nomenclature, isocyanoacetate, isocitrate, primary alcohol, isocaproate, direct conversion, isobutyrate, isoaspartate, low molecular weight, isoamyl nitrite, isethionate, electrophile, ioxitalamate, formate, ioxaglate, reverse reaction, iothalamate, carboxylate, iodoacetate, physical mean, iodite, secondary amine, interesterification, inosinate, polyethylene terephthalate, iminoester, wavenumber, iminoacetate, mild condition, imidodiphosphate, butanol, imidazolonepropionate, condensation reaction, ibotenate, scale application, ibandronate, equilibrium constant, hypoiodite, boric acid, hypofluorite, grignard reagent, hypobromite, hydroxypyruvate, sulfur atom, hydroxyphenylpyruvate, durian, hydroxymethylglutarate, nitroglycerin, hydroxyglutarate, benzene ring, hydroxyethyl methacrylate, lewis acid, hydroxycinnamate, formic acid, hydroxybutyrate, carboxyl, 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