3887-19-2 Usage
Uses
Used in Pharmaceutical Synthesis:
Ethanone, 2-(4-nitrophenyl)-1-(4-pyridinyl)is used as a key intermediate in the synthesis of pharmaceuticals and organic compounds. Its unique structure allows for the development of new drugs and therapeutic agents with potential applications in various medical fields.
Used in Chemical Reactions as a Reagent:
Ethanone, 2-(4-nitrophenyl)-1-(4-pyridinyl)serves as a reagent in various chemical reactions, facilitating the formation of desired products. Its presence of nitro and pyridinyl groups makes it a valuable tool in organic synthesis, enabling the creation of complex organic compounds with specific properties.
Used in Medicinal Chemistry Research:
Ethanone, 2-(4-nitrophenyl)-1-(4-pyridinyl)is utilized in medicinal chemistry research for the development of new drugs and therapeutic agents. Its structural features allow for the exploration of novel chemical spaces and the design of molecules with improved pharmacological properties.
Used in the Production of Complex Organic Compounds:
As a building block, Ethanone, 2-(4-nitrophenyl)-1-(4-pyridinyl)- is employed in the production of various complex organic compounds. Its versatility and reactivity make it an essential component in the synthesis of advanced materials and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 3887-19-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,8 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3887-19:
(6*3)+(5*8)+(4*8)+(3*7)+(2*1)+(1*9)=122
122 % 10 = 2
So 3887-19-2 is a valid CAS Registry Number.
3887-19-2Relevant academic research and scientific papers
An improved and practical procedure for the synthesis of substituted phenylacetylpyridines
Journet, Michel,Cai, Dongwei,Larsen, Robert D.,Reider, Paul J.
, p. 1717 - 1720 (2007/10/03)
A general procedure for the synthesis of substituted phenylacetylpyridines in excellent yields is described using a Horner-Emmons condensation between α-aminoalkylphosphonates of pyridinecarboxaldehydes and benzaldehydes with cesium carbonate at room temperature.
