Journal of the Chemical SocietyThe Society., 1949 |
From inside the book
Results 1-3 of 80
Page 1087
... formed colourless crystals , m . p . 125-126 ° ( 90 g . ) . Avery and Maclay ( loc . cit . ) , who prepared the anhydride from the same acid by heating under pressure with acetyl chloride , give m . p . 126.5 ° . a - Phenyl - a - indan ...
... formed colourless crystals , m . p . 125-126 ° ( 90 g . ) . Avery and Maclay ( loc . cit . ) , who prepared the anhydride from the same acid by heating under pressure with acetyl chloride , give m . p . 126.5 ° . a - Phenyl - a - indan ...
Page 1088
Chemical Society (Great Britain). mirror normally formed on the walls of the vessel . The mixture was then boiled with charcoal , and filtered . B - Phenyl - 1 - B - indanylpropionamide ( 0.9 g . ) formed colourless needles , from ...
Chemical Society (Great Britain). mirror normally formed on the walls of the vessel . The mixture was then boiled with charcoal , and filtered . B - Phenyl - 1 - B - indanylpropionamide ( 0.9 g . ) formed colourless needles , from ...
Page 1258
... formed colourless plates from water , m . p . 165 ° ( Found : C , 58.0 ; H , 5 · 4 ; N , 36-0 . C1 , H12N requires C , 57-9 ; H , 5 · 3 ; N , 36.8 % ) . 2- ( 6 ' - Quinolylguanidino ) -4 - hydroxy - 6 - methylpyrimidine Dihydrochloride ...
... formed colourless plates from water , m . p . 165 ° ( Found : C , 58.0 ; H , 5 · 4 ; N , 36-0 . C1 , H12N requires C , 57-9 ; H , 5 · 3 ; N , 36.8 % ) . 2- ( 6 ' - Quinolylguanidino ) -4 - hydroxy - 6 - methylpyrimidine Dihydrochloride ...
Other editions - View all
Common terms and phrases
4-dinitrophenylhydrazone absorption acetic anhydride acetone acetyl acidified added aldehyde alkaline aluminium chloride Amer amine ammonia aniline aqueous sodium atom benzene boiling bromine Calc carbon catalyst CH₂ Chem chloroform citrinin colourless needles compound condensation containing cooled crystallised crystallised from alcohol crystals cyanide cyclisation decomp derivative dilute dissolved distilled dried electrode ester evaporated extracted with ether filtered filtrate formed colourless Found fraction gave give heated under reflux hydrochloric acid hydrogen chloride hydrolysis iodide isolated ketone lactone light petroleum b. p. m. p. and mixed methanol method methyl alcohol minutes mixed m. p. mixture molecule obtained oxide phenol phosphoric picrate potassium hydroxide precipitate prepared pyridine reaction reduced pressure requires residue resin room temperature salt separated sodium hydroxide solid soluble solution solvent specimen structure substance sulphuric acid triethylamine values washed yellow needles yield