54534-72-4

Usage

Physical appearance

yellow crystalline powder

Primary uses

manufacturing of pharmaceuticals, organic synthesis

Known properties

antibacterial, antimicrobial

Common applications

ingredient in sunscreens, other cosmetic products

Potential use

photosensitizer in photodynamic therapy for cancer treatment

Safety precautions

harmful if ingested or inhaled, can cause skin and eye irritation

Upstream product

• 55501-45-6 2-chloro-N-(4-nitrophenyl)benzamide 
• 2011-66-7 2'-chloro-5-nitro-2-aminobenzophenone 

Downstream Products

• 113456-71-6 [2-(4-methyl-1-piperidinyl)-5-nitrophenyl]-(2-chlorophenyl)-methanone 
• 126377-92-2 <5-nitro-2-<(1,1-dimethylethyl)amino>phenyl>(2-chlorophenyl)methanone 
• 126377-95-5 N-[4-tert-Butylamino-3-(2-chloro-benzoyl)-phenyl]-acetamide 
• 126377-93-3 <5-amino-2-<(1,1-dimethylethyl)amino>phenyl>(2-chlorophenyl)methanone 
• 20061-59-0 2-nitroxanthone 

Relevant academic research and scientific papers

(Benzoylphenyl)piperidines: A new class of immunomodulators

A series of (benzoylphenyl)piperidines has been synthesized and evaluated for activity as immunomodulators. Several of these compounds show good activity in primary screening on the basis of the lymphocytes mitogenic response to Con A, PHA, and PWM. A chloro group in position 4 of the benzoyl moiety as well as an amino group (or a carbamate derivative) para to the piperidine nucleus seems to be essential for activity. The depicted compounds may be considered as the first examples of a new series of immunomodulators.

Pyrazolobenzazepines

There are presented compounds of the formulas STR1 wherein R1 is hydrogen or lower alkyl; R2 and R3 are selected from the group consisting of hydrogen, lower alkyl, C2 to C7 carboxylic acids, hydroxy