33864-03-8

Basic information

• Product Name: Pyridine, 3-(5-(p-methoxyphenyl)-2-oxazolyl)-
• CAS NO: 33864-03-8
• Molecular Weight: 252.272
• Mol File: 33864-03-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Pyridine, 3-(5-(p-methoxyphenyl)-2-oxazolyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyridine, 3-(5-(p-methoxyphenyl)-2-oxazolyl)-(33864-03-8)
• EPA Substance Registry System: Pyridine, 3-(5-(p-methoxyphenyl)-2-oxazolyl)-(33864-03-8)

Safety Data

• Hazardous Substances Data: 33864-03-8(Hazardous Substances Data)

Upstream product

• 4195-27-1 N-[2-(4-benzyloxy-phenyl)-2-oxo-ethyl]-nicotinamide 
• 4674-98-0 2-methyl-4-[4-(2-pyridin-3-yl-oxazol-5-yl)-phenoxy]-butane-2,3-diol 
• 123-11-5 4-methoxy-benzaldehyde 
• 626-60-8 3-Chloropyridine 
• 1011-51-4 5-(4-methoxyphenyl)-1,3-oxazole 
• 626-55-1 3-Bromopyridine 
• 99906-16-8 3-{5-[4-(2,3-dihydroxy-3-methyl-butoxy)-phenyl]-oxazol-2-yl}-1-methyl-pyridinium; chloride 
• 4195-29-3 3-[5-(4-benzyloxy-phenyl)-oxazol-2-yl]-pyridine 
• 40513-43-7 2-amino-1-(4-methoxy-phenyl)-ethanone 
• 59-67-6 nicotinic acid 
• 10400-19-8 3-pyridinecarbonyl chloride 
• 6595-28-4 2-azido-1-(4-methoxyphenyl)ethan-1-one 
• 4122-63-8 N-[2-(4-methoxy-phenyl)-2-oxo-ethyl]-nicotinamide 
• 55275-61-1 2-amino-1-(4-methoxyphenyl)ethanol 

Downstream Products

• 34433-52-8 5-[5-(4-methoxy-phenyl)-oxazol-2-yl]-1-methyl-pyridinium; iodide 
• 17190-80-6 5-(4-[(3-methylbut-2-en-1-yl)oxy]phenyl)-2-(pyridin-3-yl)oxazole 
• 4210-82-6 halfordinol 
• 89764-17-0 (E)-5-(4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]phenyl)-2-(pyridin-3-yl)oxazole 

Relevant articles and documents

Structure-Activity Relationships of New Natural Product-Based Diaryloxazoles with Selective Activity against Androgen Receptor-Positive Breast Cancer Cells

Targeted therapies for ER+/PR+ and HER2-amplified breast cancers have improved patient survival, but there are no therapies for triple negative breast cancers (TNBC) that lack expression of estrogen and progesterone receptors (ER/PR), or amplification or

Ligandless microwave-assisted Pd/Cu-catalyzed direct arylation of oxazoles

(Chemical Equation Presented) An efficient microwave-assisted palladium/copper co-mediated direct arylation of oxazoles with aryl bromides under ligandless conditions has been developed. The method is functional group tolerant and provides rapid access to medicinally relevant compounds in good yields. Coupled to the van Leusen oxazole ring synthesis, this methodology is illustrated by an expedient two-step synthesis of the four 2,5-diaryloxazole alkaloids texamine, texaline, balsoxin, and O-Me-halfordinol from commercially available starting materials.

Combinatorial discovery of novel fluorescent dyes based on Dapoxyl

We have developed a combinatorial method for the fast and effective synthesis of a library based on a known fluorescent dye, Dapoxyl using parallel solution-phase chemistry. By screening the 140 new compounds using fluorescence-based assays, we identified three new fluorescent dyes with novel properties.