35471-28-4

Upstream product

• 105-67-9 2,4-Xylenol 

Downstream Products

• 21571-69-7 (2,4-dimethyl-phenoxy)-acetone 
• 34135-75-6 2,4-dimethylphenoxyethanol 
• 63403-18-9 α-(2,4-dimethyl-phenoxy)-isovaleric acid ethyl ester 
• 176450-08-1 ethyl 2-(2,4-dimethylphenoxy)acetate 
• 130336-33-3 (+/-)-trans-2-(2,4-dimethylphenoxy)cyclohexan-1-ol 
• 6307-24-0 3-(2,4-dimethyl-phenoxy)-dihydro-furan-2-one 
• 34591-37-2 (E)-2-(3-phenylprop-2-enyl)-4,6-dimethylphenol 
• 449778-70-5 4-(2,4-dimethylphenoxy)benzonitrile 
• 872275-66-6 2,4-dimethyl-6-(2-nitro-phenylsulfanyl)-phenol 
• 117575-26-5 α-[(2,4-Dimethylphenoxy)methyl]-4-pyridinemethanol hydrochloride 
• 134160-87-5 methyl α-methoximino-α-[2-(2,4-dimethyl-phenoxy-methyl)-phenyl]-acetic acid 
• 198835-49-3 [2-(2-hydroxy-3,5-dimethylphenyl)-5,10,15,20-tetraphenylporphyrinato]copper(II) 
• 13334-49-1 2-(2,4-dimethylphenoxy)acetic acid 
• 13359-25-6 2,4-Dimethyl-phenoxyacethydroxamsaeure 

Relevant academic research and scientific papers

Aryloxymethyl derivatives of nitrogenous heterocyclic methanols and ethers thereof

Novel heterocyclicmethanols are disclosed having the formula: STR1 wherein Z is pyrrolidinyl, piperidinyl, homopiperidinyl or pyridinyl; R1 is hydrogen, loweralkyl or carbethoxymethyl; R2 is hydrogen, loweralkyl, cycloalkyl, phenyl or phenyl-loweralkyl; R3 is 1 or 2-naphthalenyl, 2,3-dihydroinden-4 or 5-yl, phenyl or phenyl substituted by loweralkyl, loweralkoxy, halogen, trifluoromethyl, phenyl, methylenedioxy, nitro, amino, loweralkylamino, diloweralkylamino, loweracylamino; the 1-position of 2-pyrrolidinyl, 2-piperidinyl or 2-homopiperidinyl may be substituted by an R4 loweralkyl group, or R1 may form methylene or --CH2 -C(O)-bridges with R4 ; the pharmaceutically acceptable salts and diastereomers thereof, which compounds have antiarrhythmic and/or hypotensive activity in animals.