1396390-73-0

Basic information

• Product Name: 2-(2-(prop-2-yn-1-yloxy)phenyl)benzothiazole
• Synonyms: 2-(2-(prop-2-yn-1-yloxy)phenyl)benzothiazole
• CAS NO: 1396390-73-0
• Molecular Weight: 265.335
• Mol File: 1396390-73-0.mol

Chemical Properties

• CAS DataBase Reference: 2-(2-(prop-2-yn-1-yloxy)phenyl)benzothiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-(prop-2-yn-1-yloxy)phenyl)benzothiazole(1396390-73-0)
• EPA Substance Registry System: 2-(2-(prop-2-yn-1-yloxy)phenyl)benzothiazole(1396390-73-0)

Safety Data

• Hazardous Substances Data: 1396390-73-0(Hazardous Substances Data)

Upstream product

• 3411-95-8 2-(benzothiazol-2-yl)phenol 
• 106-96-7 propargyl bromide 

Downstream Products

• 1396390-31-0 5-((2-(benzo[d]thiazol-2-yl)phenoxy)methyl)-3-p-tolylisoxazole 
• 1396390-34-3 5-((2-(benzo[d]thiazol-2-yl)phenoxy)methyl)-3-(4-methoxyphenyl)isoxazole 
• 1396390-58-1 2-(2-((1-(3-chloro-4-fluorophenyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)benzo[d]thiazole 
• 1396390-55-8 2-(2-((1-(4-fluorophenyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)benzo[d]thiazole 
• 1396390-61-6 2-(2-((1-(3-(trifluoromethyl)phenyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)benzo[d]thiazole 
• 1396390-36-5 5-((2-(benzo[d]thiazol-2-yl)phenoxy)methyl)-3-(2-fluorophenyl)isoxazole 
• 1396390-64-9 2-(2-((1-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)-1H-1,2,3-trizol-4-yl)methoxy)phenyl) benzo[d]thiazole 
• 1396390-42-3 5-((2-(benzo[d]thiazol-2-yl)phenoxy)methyl)-3-(4-bromophenyl)isoxazole 
• 1396390-67-2 2-(2-((1-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)-1H-1,2,3-trizol-4-yl)methoxy)phenyl)benzo[d]thiazole 
• 1396390-52-5 2-(2-((1-phenyl-1H-1,2,3-triazol-4-yl)methoxy)phenyl)benzo[d]thiazole 
• 1396390-39-8 5-((2-(benzo[d]thiazol-2-yl)phenoxy)methyl)-3-(4-chlorophenyl)isoxazole 
• 1396390-49-0 5-((2-(benzo[d]thiazol-2-yl)phenoxy)methyl)-3-(3,4,5-trimethoxyphenyl)isoxazole 
• 1396390-45-6 5-((2-(benzo[d]thiazol-2-yl)phenoxy)methyl)-3-(4-(trifluoromethoxy)phenyl)isoxazole 

Relevant articles and documents

Highly selective fluorescent probe for detection and visualization of palladium ions in mixed aqueous media

A highly selective fluorescent probe based on hydroxyphenyl-benzothiazole is synthesized which shows palladium-mediated cleavage to produce fluorescence changes at two different wavelengths in mixed aqueous media. The Royal Society of Chemistry 2013.

Silver(i)-organic frameworks assembled with flexible supramolecular synthons with a pendant ethynide arm attached to the heteroaryl skeleton

The reactions of flexible supramolecular synthons with a pendant ethynide arm attached to a heteroaryl skeleton and different silver(i) salts under solvent evaporation conditions yielded four silver-organic frameworks. In 1-4, the Ag7, Ag8 and Ag9 aggregates are fused together through trifluoroacetate groups and/or Ag-N coordination bonds to generate a 2D layer, and finally linked into 3D supramolecular networks by argentophilic interactions or hydrogen bonding. The diversities of the present structures also indicate that both solvent and the anionic component play vital roles in the assembly of silver(i)-ethynide complexes. In addition, their luminescence behaviors have been studied in the solid state.

Triazole-Coupled Benzimidazole-Based Fluorescent Sensor for Silver, Bromide, and Chloride Ions in Aqueous Media

A triazole-coupled benzimidazole-based fluorescent probe S1 with nitrogen and oxygen binding sites was synthesized and its properties as a probe for cations were investigated. Probe S1 was found to be highly selective toward Ag+ ions in aqueous

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Cancer is a major health problem and the most upsetting disease in humans, leading to death in both developed and developing countries. Proper treatment of the disease is still a challenge. Chemotherapy is considered one of the regimens to cure this disea

Synthesis and biological evaluation of novel triazoles and isoxazoles linked 2-phenyl benzothiazole as potential anticancer agents

A new series of isoxazoles and triazoles linked 2-phenyl benzothiazole were synthesized and evaluated for their anticancer activity. These compounds have been tested for their cytotoxicity three cancer cell lines. Among the compounds tested, compound 5d s