1310 



ACIDS C,H,404 



Suberic acid 



■ Synthesis and Nitrile 

 CN . CBICE,-]^ . CHjCN 



Hamonet, AlieJ. Paris, C.-R. Ac 

 •!., 136, 1903, (244-246). 



/-a-Isopropyl-glutaric acid <^8Hi404 



Semmler, F. W[il]ielm]. Berlin, Ber. 

 i). diem. Ges., 36, 1903, (1749-1 75G). 



Trimetliylglutaric acid 



CO2H . CMe2 . CH2 . CHMe . CO2H 



and the dihromo-derivative 



CO2H . CMej . CHBr . CMeBr . COjH 



Perkin, W. H. jun. and Smith, Aliie 

 E. [007-Trinietliylgliitaric acid and its 

 /37-dibromo-derivative.] London, J. 

 Chem. Soc, 83, 1903, (771-779j; 

 [Abstrac't] Proe. Chem. Soc, 19, 1903, 

 (163). 



ACID CoHi„04 



a, a, a'-Trimethyladipic acid 

 CO2H . CHMe . Cilj . CII2 . CMe, . CO2H 



WaUach, 0. Liebigs Ann. Chem., 

 Leipzig, 329, 1903,(82-108). 



566 1310 



ACID C,3H,404 



Ketooxystearic acid 



CH3 . [CH2]7 . CO . CH(OH) . [CH2], . CO2H 



or 

 CH3[CH2]7 . CH(OH) . CO . [CHj], . CO2H 



Holde, D[avid] und Marcusson, J. 

 Berlin, Ber. D. chem. Ges., 36, 1903, 



(2657-2GC2). 



PARAFFIN ACIDS WITH F1\'E 

 OXYGEN ATOMS. 



ACIDS CnH2..-205 



ACIDS C4H6O5 



Malic acid 



CO2H . CH2 . CH(OH) . CO2H 



Heide, Hermaim v. d. Ueber zwei 

 V'erbiudimgen der 1. Aepfelsaure mit 

 tlen beiden aktiveu Weinsauren uebst 

 Beitriigen zur Erklanmg der Aenderiing 

 des Drehvennogens dieser beiden Sau- 

 ren. Diss. Berlin. Bex-lin-Charlotten- 

 bnrg (Drack v. J. Zalachowski), [1903], 

 (39, mit 1 Taf.). 21 em. 



Grosz, Imre. L'eber die Erzeugung 

 der Aepfelsaure. (Ungarisch)Budai)est, 

 1903,(24). 22 cm. 



ACIDS CiuHia04 



a-Methyl-a'-isopropyl-adipic acid 



C8H,6(C02H)2 



Metliyl and ethyl esters, chloride, 

 aimde, anilide, and ■p-toluidc 



Martine, C. Preparation de qnelqiies 

 cumbiuaisons de I'acide o methyl a iso- 

 propvladipiqiie. Paris, C.-R. Acad, sci., 

 136, '1903, (458-459). 



ACID CnH,,04 



Ennane dicarboxylic acid 



C02H.[CH2lg.C02lI 



Zukov, A^ A. et Sestakov, P. 1. St. 

 Peterburg, Zurn. nxss. fiz.-chiui. ObSC, 

 35, 1903, (1-22). 



Amide. 



McCrae, John. The rotatory power of 

 maldiamide, maldi-n-propylamide, and 

 maldibenzylamide. London, J. Chem. 

 Soc, 83, 1903, (1324-1327); [Abstract] 

 Proc. Chem. Soc, 19, 1903, (230-231). 



l-Maldi-n-p7-opylamide C10H20O3N2 



McCrae, John. Loudon, J. Chem. 

 Soc, 83, 1903, (1324-1327) ; [Ahstract] 

 Proc Chem. Soc, 19, 1903, (230-231). 



I-Mtddibeiizylamkle C13H20OJN2 



McCrae, John London, J. Chem. 

 Soc, 83, 1903, (1324-1327;; [Abstract] 

 Proc. Chem. Soc, 19, 1903, (230-231). 



