24021-68-9

Upstream product

• 186581-53-3 diazomethane 
• 26077-80-5 (4-benzoylphenyl)acetic acid 
• 98-88-4 benzoyl chloride 
• 101-41-7 benzeneacetic acid methyl ester 
• 53689-84-2 4-acetylbenzophenone 
• 39148-58-8 4-benzoylbenzoyl chloride 
• 33238-47-0 4-diazoacetyl-benzophenone 
• 42327-85-5 (4-benzoyl-phenyl)-acetic acid amide 

Downstream Products

• 26077-80-5 (4-benzoylphenyl)acetic acid 
• 151389-72-9 [4-(Hydroxy-phenyl-methyl)-phenyl]-acetic acid methyl ester 
• 152656-35-4 [4-(Amino-phenyl-methyl)-phenyl]-acetic acid methyl ester 
• 152656-05-8 [4-(Chloro-phenyl-methyl)-phenyl]-acetic acid methyl ester 
• 152656-17-2 [4-(Azido-phenyl-methyl)-phenyl]-acetic acid methyl ester 
• 152655-31-7 {4-[(4-Chloro-benzenesulfonylamino)-phenyl-methyl]-phenyl}-acetic acid methyl ester 
• 89709-54-6 (4-Benzoyl-phenyl)-acetic acid (3S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 

Relevant academic research and scientific papers

HETEROAROMATIC RING COMPOUNDS

Heteroaromatic ring compounds or pharmaceutically acceptable salts thereof, which have excellent characteristics and have strong curative effects to immuno-imbalance and choronic inflammation. Representative is the compound of the formula:

Synthesis and thoromboxane A2 antagonistic activity of [[1-aryl(or benzyl)-1-(benzenesulfonamido)methyl]phenyl]alkanoic acid derivatives

In order to find a new antiasthmatic and antithrombotic agents, various [[1-aryl(or benzyl)-1-(benzenesulfonamido)methyl]phenyl]alkanoic acid derivatives were synthesized. Evaluation of these compounds for thromboxane A2 (TXA2) antag

Liquid Crystalline Properties of Cholesteryl ω-Arylalkanoates

The thermal properties of the homologous series of cholesteryl ω-(4-benzoylphenyl)- (I), ω-(4-benzylphenyl)- (II), ω-benzoyl- (III), and ω-phenoxyalkanoate (IV) have been investigated.For series I and II the cholesteric-isotropic (Ch-I) transition temperatures, enthalpies, and entropies show a remarkable alternation.For series III and IV, the transition temperatures, enthalpies, and entropies exhibit weak alternation and their trends are opposite to those for series I and II, and the cholesteryl ω-phenylalkanoates.The cholesteric-isotropic transition temperatures are discussed in terms of the geometrical and electrical alternations stemming from the terminal aryl groups, and also the relative importance between these two terms.