78235-16-2

Upstream product

• 78235-15-1 ethyl <2,3-dichloro-4-<4-hydroxy-3-<(2-chloroacetyl)aminomethyl>benzyl>phenoxy>acetic acid 
• 107-06-2 1,2-dichloro-ethane 

Downstream Products

• 85297-72-9 Ethyl 2,3-dichloro-4-[(3'-chloroacetamidomethyl-4'-hydroxy-5'-chloro)benzoyl]phenoxy acetate 
• 78235-55-9 ethyl <2,3-dichloro-4-(3-chloro-5-<(dimethylamino)methyl>-4-hydroxybenzoyl)phenoxy>acetate 
• 78235-70-8 ethyl <2,3-dichloro-4-<3-(aminomethyl)-5-chloro-4-hydroxybenzoyl>phenoxy>acetate 
• 78235-31-1 [2,3-Dichloro-4-(3-chloro-5-dimethylaminomethyl-4-hydroxy-benzoyl)-phenoxy]-acetic acid 
• 78235-17-3 <2,3-dichloro-4-<3-chloro-4-hydroxybenzoyl>phenoxy>acetic acid 

Relevant academic research and scientific papers

[(Aminomethyl)aryloxy]acetic acid esters. A new class of high-ceiling diuretics. 1. Effects of nitrogen and aromatic nuclear substitution

A series of Mannich bases and aminomethyl derivatives of ethyl [2,3-dichloro-4-(4-hydroxybenzoyl)phenoxy]acetate were synthesized and tested for saluretic and diuretic activities. The effects of nitrogen and aromatic nuclear substitution, reorientation of

Benzophenone derivatives

Described are compounds of the formula STR1 wherein R is hydrogen, loweralkyl, aminomethyl or halo, R1 is hydroxy or NHX where X is H, loweralkyl, phenyl, substituted phenyl, acetyl, benzyl and substituted benzyl, and Y is hydrogen, loweralkyl