To confirm this, a control experiment was conducted by using benzoic acid-d5 and D2 as reactants. The mass spectrum (MS) analysis of the product shows the appearance of molecular ion peaks at m/z of 139.2 and 138.2 with the intensity ratio of 1.9, denoting the presence of 6 deuterated...
Product Name:Benzoic acid Synonyms:210;a 1 (acid);Acide benzoique;Benzoic aBenzoic acidcid;Mefenamic Acid Impurity D;Benzyl acid;SS Benzoic Acid;Glycopyrronium Bromide EP Impurity D CAS:65-85-0 MF:C7H6O2 MW:122.12 EINECS:200-618-2
colorSlightly yellow to yellow-brown Water Solubility4.8g/L(25 ºC) BRN976984 InChIKeyFBRJYBGLCHWYOE-UHFFFAOYSA-N CAS DataBase Reference433-97-6(CAS DataBase Reference) NIST Chemistry Reference«alpha»,«alpha»,«alpha»-Trifluoro-o-toluic acid(433-97-6) ...
Dilution with water and filtration yields ethyl 4-(3-benzylthiopropylamino)benzoate as a white, crystalline solid. EXAMPLE 15 Preparation of sodium 4-(11-hydroxyundecylamino)benzoate A mixture of 3.62 g. of 4-(11-hydroxyundecylamino)benzoic acid and 25 ml. of ethanol-water (9:1) ...
Benzoic acid derivatives of the formula I 1 <inline-img he="36.0045" wi="63.8442" img-type="C" img-num="1"></inline-img> where X i
1. A fungicidal composition comprising as active ingredient an amount of from about 0.001 to about 95% by weight of a following acid or its salt: 3-{[5-chloro-4-(trifluoromethyl)-2-nitro]-phenoxy}-benzoic acid; 3-[2-(trifluoromethyl)-phenoxy]-benzoic acid; 3-{[2-chloro-4-(triflu...
Prepared using the procedure described above, using 4-hydrazinobenzoic acid. LCMS m/z 427.34 [M+H]+ @ RT 1.38 min, 74% purity EXAMPLE 4 3-[4-(4-Nitro-phenyl)-3-oxo-3,5-dihydro-pyrazolo[4,3-c]quinolin-2-yl]-benzoic acid Prepared by methods analogous to Example 3. LCMS m/z 42...
Cyclopentanediol and drug salts extracted from it; EU pharmaceutical ingredients include phenylacetylbenzoic acid, benzamidas, benzyl alcohol and benzoic acid derivatives as well as acceptable snakes, diluents or pharmaceutical vehicles; or compounds containing Z as COOH or its salts; or uncoms with Z...
In this process: Ar is phenyl or substituted phenyl; R1 is alkyl or alkyl substituted with halogen, amino, nitro, cyano, hydroxy, carboxy, alkoxy, thio, mercaptoalkyl or alkylthio; and R2 is alkyl, hydroxy, alkoxy, acyl, carboxylic acid and aldehyde, amide and ester derivatives thereof, ...
wherein R2, Y and m have the above-identified values, and/or with a functional acid derivative thereof, e.g., an acid halide or acid anhydride, provided that in one of the compounds II or III, m = 0. Furthermore, on compounds of or analogous to Formula I wherein hydroxyl groups ar...