Alcohols. 



471 



1230 



Pyrocatechol i 



Pyroeatechin. ' 'ateehol. 

 Jackson <S Kelley. L12039. The 

 of nitric acid on beptachli 

 catechinorthoquino bemiel 



Weinland u Denzel. 1151)7 1 115977. 

 Brenzcatecliin-Verbindungen des Alu- 

 minium* m iuins, Bowie 

 fiber einige Alkalisalze des Brenzcate- 

 chins. Verbind - Brenzcate- 

 chine mit Alkali on Carbon- 

 sauren and mil Alkali- bezw. Erdalkali- 

 Mitallsal. • i lener Sauren. 



CHLl lR< >-li Ik '-I'YROCATECHOI.. 



Dimethyl ether. 



Seer u. Ehrenreich. M., 34, (645). 



Tim ipyri >v\ i Ei ihi <i. ( V.H 4 (OH)(SH) 

 o-Phenolmercaptan. 



Siebert. L15091. 



I )ITIII« H'Y R( II \ [ T.CHOL C 6 H 4 (SH) 2 



and ii- lerivatives. Also the 



compound C„E i >.H) 2 



PoUak. M, 34. L673). 



Resorcinol C 6 H 4 (OH) 2 [l : 3] 



Resorr'ni. 



Andeer. L09082. Resorcin und seine 

 synthetischen Farbstofipraparate als 

 epileptogene Substanzen. 



Kehrmann u. Loth. 112257. Re- 

 Borcin-benzein (3-( >xy-9-phenyl-fluoron). 



Thioresoeoinol C 8 H 4 (SH)(OH) 

 Zincke u. Ebel. B., 47, .•: 



DlTBIOBESOBOIK 3B 



Diehloro derivative. 



Pollak u. Wienenberger. II.. 35, 

 I 167 



nzyl etlier. 



Finzi. 110840. Dibenziltioresi 

 aziltioidrochinone C 6 H 4 (SC 7 H 7 )j. 



Quinol C 6 H 4 (OB [1:1 

 roquinone. 



Maldiney. 113105. One reaction 

 coloree presentee par 1 nydroquinone a 

 I'etat Bolide. 



Pinnow. 114154. L'oxydatibn simul- 

 I linone et dn sulfite de 

 sodium. 



Seyewetz et Pr„ris. 115075. Les 

 hydroquinones dfuriqueset 



lenr transformation en monobroniosulfo- 

 quinones. 



I'm S 4 (OH).SB 



ind deriv 



Zincke u. Ebel. B., 47, (1100 . 



i QfOL. 



Dii i 3 7 ) 2 



Finzi. L10840. 



PHENOL C 7 H d 2 



- : 4-Dioxy-l-methylbenzene 



3 : 5 : 6-Teibeomo derivative. 



Tribromocre8orcinol. 



Blanksma. 109647. 



PHENOL C> H 



Tetradecylpyrocatechol 



C 14 H 2fl .C 6 H 3 (OH) 2 



Dimethyl ■ ther C 14 H 9 .C g B 3 OMe 



Majima <& Nakamura. 1 13102. 

 Hydrourushiol C2oH 3 40 2 



Also lead compound l 2 , di- 



benzoyl derivative C 14 B >i!z) 2 or 



C 15 H 31 .C 6 H liacetyl deri- 



rative C 14 H 29 .C 6 H 2 Br(OAc) 2 , l'ibromo- 

 and dinitroai - bisdinitro- 



benzovl derivative, and the amino- and 

 dinitro-derivatives of the dimethyl ether. 



Majima & Nakamura. 113101. 

 PHENOL C 2 ,H 3 50 2 



Pentadecylpyrocatechol 



C 15 H 31 .C s H 3 (OH) 2 [4 : 2 : lj 



DlMETHTl Kill r C 15 H ,.C II (OMe) 2 



Pentadecylveratrole. 



Majima & Nakamura. 1 13102. 

 PHENOL C ? H, 



Hexadecylpyrocatechol 



C 16 H 33 .C 6 H 3 (OH) 2 1:2:1] 



Dimethyl i »Me), 



Hexadecylveratrole. 



Majima & Nakamura. 113 



ALCOHOLS CHfi-aOi 



alcohol CH, 0: 



Phenylethylene glycol 

 C 6 H 5 .CH >fl CH, "II 



Styrolerie alcohol. 



Evans & Morgan. 110727. The 

 preparation and the oxidation of styro- 

 lene alcohol. 



