55274-11-8

Upstream product

• 555-16-8 4-nitrobenzaldehdye 
• 603-35-0 triphenylphosphine 
• 32752-54-8 4-(bromomethyl)benzophenone 

Downstream Products

• 75344-81-9 cis-4-(p-nitrostyryl)benzophenone 
• 75344-80-8 trans-4-(p-nitrostyryl)benzophenone 
• 20488-45-3 cis-4-Benzoylstilbene 
• 20488-44-2 (E)-2-(4'-benzoylphenyl)-1-phenyl-ethene 
• 75344-79-5 cis-4-(2,4-dichlorostyryl)benzophenone 
• 75344-79-5 trans-4-(2,4-dichlorostyryl)benzophenone 
• 882429-54-1 (E)-2-[(3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-Acetoxy-3,11-dihydroxy-4,8,10,14-tetramethyl-hexadecahydro-cyclopenta[a]phenanthren-(17Z)-ylidene]-6-(4-benzoyl-phenyl)-hex-5-enoic acid 2,2-dimethyl-propionyloxymethyl ester 
• 882429-61-0 2-[(3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-Acetoxy-3,11-dihydroxy-4,8,10,14-tetramethyl-hexadecahydro-cyclopenta[a]phenanthren-(17Z)-ylidene]-6-(4-benzoyl-phenyl)-hexanoic acid 2,2-dimethyl-propionyloxymethyl ester 
• 3139-85-3 4-vinylbenzophenone 

Relevant academic research and scientific papers

CARBONYLPHENACENE COMPOUND, ORGANIC LUMINESCENT MATERIAL, ORGANIC SEMICONDUCTOR MATERIAL AND METHOD OF PRODUCING CARBONYLPHENACENE COMPOUND

PROBLEM TO BE SOLVED: To provide novel compounds which have resistance to external environments, such as high voltages and oxygen, and are usable in organic semiconductor materials, etc. and a method of producing such novel compounds efficiently. SOLUTION

Control of chain ends of polyesters in polycondensation of AA and BB monomers by use of solid-phase reagent

For selective synthesis of linear polyester having a functional group at one end, polycondensation between 1,4-butanediol (1a) and sebacoyl chloride (2a) and between 1,12-dodecanediol (1b) and isophthaloyl chloride (2b) was conducted in the presence of ox

Synthesis and biological evaluation of photoaffinity labeled fusidic acid analogues

Novel photoaffinity labeled fusidic acid analogues were obtained by a synthetic sequence employing a Wittig reaction between a fusidic acid aldehyde and benzyl bromides in the key step. Three commonly used photoreactive groups, benzophenone, trifluoromethyldiazirine, and aryl azide, were used. The photoaffinity labeled fusidic acid analogues demonstrated a potent antibacterial activity (MIC 0.016-4 μg/mL) and therefore represent a potential tool for the elucidation of the interactions between fusidic acid and its receptor EF-G.