61309-99-7

Usage

Uses

Used in Laboratory Research:
2-Methyl-6-phenylbenzoxazole is used as a fluorescent dye for labeling proteins and other biological structures. This application facilitates the visualization of these structures under a microscope, aiding researchers in their studies and analysis.
Used in Manufacturing Light-Emitting Diodes (LEDs):
In the industry, 2-Methyl-6-phenylbenzoxazole is utilized in the production of light-emitting diodes. Its chemical properties make it a valuable component in creating efficient and long-lasting LED devices.
Used in Textile Industry:
MPBO is also used in the creation of optical brighteners for textiles. These brighteners enhance the appearance of fabrics by making them appear brighter and more vivid, which is particularly beneficial in the production of visually appealing clothing and other textile products.
Safety Precautions:
Although 2-Methyl-6-phenylbenzoxazole is considered a relatively low-risk chemical, it is important to follow proper safety procedures during its use and handling. This is to ensure the protection of human health and to minimize any potential environmental impact.

Upstream product

• 811-98-3 d⁽⁴⁾-methanol 
• 151230-42-1 6-bromo-2- methylbenzo[d]oxazole 
• 98-80-6 phenylboronic acid 

Downstream Products

• 1312435-75-8 C₁₇H₁₅NO₃ 
• 61309-82-8 6-phenyl-2-[4-(2-phenyl-2H-[1,2,3]triazol-4-yl)-styryl]-benzooxazole 
• 61519-93-5 6-phenyl-2-[4-(4-phenyl-[1,2,3]triazol-2-yl)-styryl]-benzooxazole 
• 65965-26-6 2-{4-[2-(6-phenyl-benzooxazol-2-yl)-vinyl]-phenyl}-[1,2,4]triazolo[1,5-a]pyridine 
• 65965-33-5 6-chloro-2-{4-[2-(6-phenyl-benzooxazol-2-yl)-vinyl]-phenyl}-[1,2,4]triazolo[1,5-a]pyridine 

Relevant academic research and scientific papers

OXADIAZOLE DERIVATIVE HAVING ENDOTHELIAL LIPASE INHIBITORY ACTIVITY

Disclosed is a compound which is useful as an endothelial lipase inhibitor. A compound represented by the formula: its pharmaceutically acceptable salt, or a solvate thereof, wherein Ring A is aromatic carbocycle or aromatic heterocycle,Z is —NR5—, —O— or —S—,R5 is hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aryl or the like,R1 is hydrogen, halogen, hydroxy, cyano, nitro, carboxy, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl or the like,R2 and R3 are each independently hydrogen, halogen, hydroxy or the like,R4 is a group represented by the formula: —(CR6R7)n-R8, wherein R6 and R7 are each independently hydrogen, halogen, hydroxy or the like, n is an integer of 0 to 3, R8 is carboxy, cyano, substituted or unsubstituted alkyl or the like, Rx is halogen, hydroxy, cyano, nitro, carboxy, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl or the like,m is an integer of 0 to 3.

Nucleophilic Aromatic Substitution on Ester Derivatives of Carcinogenic N-Arylhydroxamic Acids by Aniline and N,N-Dimethylaniline

Decomposition of N-(pivaloyloxy)-2-(acetylamino)fluorene (1b) and N-(sulfonatooxy)-4-(acetylamino)biphenyl (2a) in MeOH occurs predominately via N-O bond cleavage to yield oxazoles (5, 6, 23), methoxy adducts (7, 8, 24, 25, 26), and rearrangement products