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Propoxycaine

C21HJ0O2 22034-63-5) see Promestriene 2-propoxy-4-nitrobenzoic acid methyl ester (CiiHijNO,) see Propoxycaine propylamine... [Pg.2438]

C Hi N I07-W-H) see Carticaine Cropropamide Etidocaine Prilocaine Propafenone propyl benzenesulfonate (CjHijOjS KO-42-2) see Propoxycaine propyl bromide... [Pg.2438]

Closely related drug molecules Proxymetacaine, benzocaine, amethocaine, butacaine, propoxycaine, procainamide (for stability of an amide group see paracetamol), bupivacaine, lignocaine, prilocaine. [Pg.40]

The acid (9) is used in the synthesis of a number of local anaesthetics such as Propoxycaine (10). The amino group cannot be put in by nitration of salicyclic acid (11) as the oxygen atom will direct o,p and give the wrong isomer. The problem can be solved by deliberately making the wrong isomer and nitrating that. [Pg.26]

See other pages where Propoxycaine is mentioned: [Pg.10]    [Pg.443]    [Pg.275]    [Pg.245]    [Pg.1734]    [Pg.2350]    [Pg.2419]    [Pg.2427]    [Pg.2427]    [Pg.29]    [Pg.462]    [Pg.487]    [Pg.2350]    [Pg.2427]    [Pg.2427]    [Pg.138]    [Pg.174]    [Pg.198]    [Pg.218]    [Pg.936]    [Pg.936]    [Pg.936]    [Pg.937]    [Pg.1077]    [Pg.1079]    [Pg.1087]    [Pg.1096]    [Pg.1099]    [Pg.1102]    [Pg.1108]    [Pg.1115]    [Pg.1126]    [Pg.1128]    [Pg.1147]    [Pg.1155]    [Pg.1559]    [Pg.266]    [Pg.2117]    [Pg.234]    [Pg.234]    [Pg.261]   
See also in sourсe #XX -- [ Pg.10 ]

See also in sourсe #XX -- [ Pg.10 ]

See also in sourсe #XX -- [ Pg.1734 ]

See also in sourсe #XX -- [ Pg.261 ]

See also in sourсe #XX -- [ Pg.140 , Pg.157 , Pg.159 ]



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Propoxycaine hydrochloride

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