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2-(2-pyridylphenyl)-1,3-dioxolane, also known as PPD, is a chemical compound with a unique structure consisting of a pyridine ring attached to a phenyl group within a dioxolane ring. It is commonly used as a ligand in coordination chemistry and as a building block in organic synthesis. PPD has been studied for its potential applications in various fields including pharmaceuticals, agriculture, and materials science. It exhibits interesting properties that make it a valuable tool for designing new molecules with specific functions. However, as with any chemical compound, proper handling and safety precautions should be taken to avoid any potential health hazards associated with its use.

150711-15-2

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150711-15-2 Usage

Uses

Used in Coordination Chemistry:
2-(2-pyridylphenyl)-1,3-dioxolane is used as a ligand for forming coordination complexes with metal ions. Its unique structure allows for the creation of stable complexes that can be used in various applications, such as catalysis and sensing.
Used in Organic Synthesis:
2-(2-pyridylphenyl)-1,3-dioxolane is used as a building block in the synthesis of more complex organic molecules. Its versatile structure can be incorporated into a wide range of compounds, making it a valuable component in the development of new pharmaceuticals, agrochemicals, and materials.
Used in Pharmaceutical Applications:
2-(2-pyridylphenyl)-1,3-dioxolane is used as a starting material or intermediate in the synthesis of pharmaceutical compounds. Its unique structure can be modified to create new drugs with specific therapeutic properties, such as improved efficacy or reduced side effects.
Used in Agricultural Applications:
2-(2-pyridylphenyl)-1,3-dioxolane is used as a component in the development of new agrochemicals, such as pesticides and herbicides. Its potential to form stable complexes with metal ions can be exploited to create compounds with enhanced activity and selectivity.
Used in Materials Science:
2-(2-pyridylphenyl)-1,3-dioxolane is used in the design and synthesis of new materials with specific properties, such as improved conductivity, stability, or optical characteristics. Its unique structure can be incorporated into polymers, composites, or other materials to enhance their performance in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 150711-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,7,1 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 150711-15:
(8*1)+(7*5)+(6*0)+(5*7)+(4*1)+(3*1)+(2*1)+(1*5)=92
92 % 10 = 2
So 150711-15-2 is a valid CAS Registry Number.

150711-15-2Downstream Products

150711-15-2Relevant academic research and scientific papers

The First Synthesis of Pyridophthalazinium System and its Three Thieno-fused Analogues

Gronowitz, Salo,Messmer, Andras,Timari, Geza

, p. 1049 - 1052 (2007/10/02)

Substituted biaryl 9, 14-16 were synthesized through Pd(0)-catalyzed cross coupling reactions between boronic acids or tin derivatives and aryl halides.N-Amination, and subsequent ring closure resulted in the new angularly-fused pyridopyridazinium systems 1-4.The use of silver oxide as a cocatalyst in the couplings of tin derivatives was essential in order to obtain rapid reaction and better yields.Structures were determined by 1H nmr and 13C nmr spectra.

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