55274-11-8

Basic information

• Product Name: Phosphonium, [(4-benzoylphenyl)methyl]triphenyl-, bromide
• CAS NO: 55274-11-8
• Molecular Formula: C32H26OP.Br
• Molecular Weight: 537.436
• Mol File: 55274-11-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Phosphonium, [(4-benzoylphenyl)methyl]triphenyl-, bromide(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonium, [(4-benzoylphenyl)methyl]triphenyl-, bromide(55274-11-8)
• EPA Substance Registry System: Phosphonium, [(4-benzoylphenyl)methyl]triphenyl-, bromide(55274-11-8)

Safety Data

• Hazardous Substances Data: 55274-11-8(Hazardous Substances Data)

Upstream product

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

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 
• 3139-85-3 4-vinylbenzophenone 
• 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 
• 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 
• 75344-79-5 cis-4-(2,4-dichlorostyryl)benzophenone 
• 75344-79-5 trans-4-(2,4-dichlorostyryl)benzophenone 

Relevant articles and documents

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

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.