- propiophenone
- pro·pio·phe·none
English syllables. 2014.
propiophenone
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Propiophenone — Chembox new Name = Propiophenone ImageFile = Propiophenone.png ImageName = Propiophenone IUPACName = 1 Phenylpropan 1 one OtherNames = Ethyl phenyl ketone Section1 = Chembox Identifiers SMILES = CCC(C1=CC=CC=C1)=O CASNo = 93 55 0 RTECS = Section2 … Wikipedia
propiophenone — propiofenonas statusas T sritis chemija formulė C₆H₅COCH₂CH₃ atitikmenys: angl. propiophenone rus. пропиофенон ryšiai: sinonimas – 1 fenil 1 propanonas … Chemijos terminų aiškinamasis žodynas
propiophenone — noun The ketone CH CO CH CH; ethyl phenyl ketone … Wiktionary
propiophenone — pro·pio·phe·none .prō pē ō fē .nōn, fen .ōn n a flowery smelling compound C9H10O used in perfumes and in the synthesis of pharmaceuticals (as ephedrine) and organic compounds … Medical dictionary
propiophenone — ˌprōpēōˈfēˌnōn, ˈfenˌōn, ˌōfəˈnōn noun ( s) Etymology: International Scientific Vocabulary propio + phenyl + one : a flowery smelling compound C9H10O used in perfumes and in the synthesis of pharmaceuticals (as ephedrine) and organic compounds … Useful english dictionary
Cathinone — Drugbox IUPAC name = (S) 2 amino 1 phenyl 1 propanone width = 175px CAS number=71031 15 7 ATC prefix= ATC suffix= ATC supplemental= PubChem= DrugBank= C=9 | H=11 | N=1 | O=1 molecular weight = 149.19 g/mol bioavailability= metabolism =… … Wikipedia
Dimethylcathinone — Drugbox IUPAC name = 2 dimethylamino 1 phenylpropan 1 one width= 200 CAS number= 15351 09 4 ATC prefix= ATC suffix= PubChem= 71872 DrugBank= C=11 | H=15 | N=1 | O=1 molecular weight = 177.243 bioavailability= metabolism = elimination half life=… … Wikipedia
Methcathinone — Systematic (IUPAC) name (RS) … Wikipedia
Oxime — An oxime is a chemical compound belonging to the imines, with the general formula R1R2C=NOH, where R1 is an organic side chain and R2 may be hydrogen, forming an aldoxime, or another organic group, forming a ketoxime. O substituted oximes form a… … Wikipedia
Phenylpropanolamine — Systematic (IUPAC) name 2 … Wikipedia
